Allele Registry

Canonical Allele Identifier: PA2825101678

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000823666

RCV002336725

ClinVar Variation:

665396

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr17Ile	CA4447937 NM_000245.4:c.50C>T