Allele Registry

Canonical Allele Identifier: PA212646

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000185580

RCV000202585

ClinVar Variation:

183686

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Phe841Val	CA212644 NM_000245.4:c.2521T>G