Allele Registry

Canonical Allele Identifier: PA261579

Gene: PTPN11 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000033478

RCV000033479

RCV000037638

RCV000037639

RCV000254683

RCV000472904

RCV000762884

RCV000856760

RCV001813246

RCV002453282

RCV003150934

ClinVar Variation:

40502

40503

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Glu76Asp	CA261577 NM_002834.5:c.228G>C CA261580 NM_002834.5:c.228G>T