Allele Registry

Canonical Allele Identifier: PA2825104086

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003369926

ClinVar Variation:

2612857

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Val1220Phe	CA368991472 NM_000245.4:c.3658G>T