Allele Registry

Canonical Allele Identifier: PA916056480

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

48976

ClinVar RCV:

RCV000033483

RCV000157021

RCV000212893

RCV001261998

RCV001813247

ClinVar Variation:

40506

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Asp106Ala	CA261584 NM_080601.3:c.317A>C