Allele Registry

Canonical Allele Identifier: PA093848

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000175410

RCV000417458

RCV000431224

ClinVar Variation:

194929

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Tyr1230His	CA241164 NM_000245.4:c.3688T>C