Allele Registry

Canonical Allele Identifier: PA916027577

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000175410

RCV000417458

RCV000431224

ClinVar Variation:

194929

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Tyr800His	CA241164 NM_001324402.2:c.2398T>C