Allele Registry

Canonical Allele Identifier: PA220139

Gene: PTPN11 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

49028

49029

571274

ClinVar RCV:

RCV000033545

RCV000033546

RCV000077852

RCV000157015

RCV000210040

RCV000515165

RCV000618529

RCV000660241

RCV000692146

RCV000762886

RCV000824749

RCV000824750

RCV001028095

RCV001374913

RCV001813261

RCV002390131

RCV003147310

RCV003147311

RCV004532494

RCV004532495

ClinVar Variation:

40558

40559

571101

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Gly503Arg	CA220137 NM_002834.5:c.1507G>A CA273459 NM_002834.5:c.1507G>C CA891844000 NM_002834.5:c.1506_1507delinsCC