Allele Registry

Canonical Allele Identifier: PA1139697020

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

969677

ClinVar RCV:

RCV001261023

RCV001813585

ClinVar Variation:

981537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Gln514Leu	CA386779920 NM_001330437.2:c.1541A>T CA645586232 NM_001330437.2:c.1541_1542delinsTT