Allele Registry

Canonical Allele Identifier: PA2829385556

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

969677

ClinVar RCV:

RCV001261023

RCV001813585

ClinVar Variation:

981537

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Gln510Leu	CA386779920 NM_002834.5:c.1529A>T CA645586232 NM_002834.5:c.1529_1530delinsTT