Allele Registry

Canonical Allele Identifier: PA916028143

Gene: PTPN11 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

49022

ClinVar RCV:

RCV000033538

RCV000156989

RCV000254685

RCV001002769

RCV001335067

RCV001813258

RCV002504856

RCV004532492

ClinVar Variation:

40552

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Pro495Leu	CA273407 NM_001330437.2:c.1484C>T