Allele Registry

Canonical Allele Identifier: PA2827312758

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

175539

ClinVar RCV:

RCV000156008

RCV000780656

ClinVar Variation:

179221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Asp61Ala	CA273600 NM_001330437.2:c.182A>C