Allele Registry

Canonical Allele Identifier: PA2825102527

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001294941

ClinVar Variation:

999003

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Arg413Pro	CA368972745 NM_000245.4:c.1238G>C