Allele Registry

Canonical Allele Identifier: PA2827313019

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

175541

ClinVar RCV:

RCV000151696

RCV000380092

RCV000654965

ClinVar Variation:

164998

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Asn200Tyr	CA273218 NM_001330437.2:c.598A>T