Allele Registry

Canonical Allele Identifier: PA2825619053

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002002894

RCV002361344

ClinVar Variation:

1482319

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Arg413Cys	CA164865824 NM_001127500.3:c.1237C>T