Allele Registry

Canonical Allele Identifier: PA916056547

Gene: PTPN11 HGNC NCBI

ClinVar RCV:

RCV000055889

RCV001064303

ClinVar Variation:

65666

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Tyr279Ser	CA344998 NM_080601.3:c.836A>C