Allele Registry

Canonical Allele Identifier: PA2827254415

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000185580

RCV000202585

ClinVar Variation:

183686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Phe411Val	CA212644 NM_001324402.2:c.1231T>G