Allele Registry

Canonical Allele Identifier: PA2825617658

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000823666

RCV002336725

ClinVar Variation:

665396

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Thr17Ile	CA4447937 NM_001127500.3:c.50C>T