Allele Registry

Canonical Allele Identifier: PA2825104094

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002349206

RCV003102432

ClinVar Variation:

1734426

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Asp1228Tyr	CA368991564 NM_000245.4:c.3682G>T