Allele Registry

Canonical Allele Identifier: PA2825102898

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000121353

RCV000206655

RCV000210762

RCV001293429

RCV001562214

RCV003945083

ClinVar Variation:

134654

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Arg591Trp	CA332158 NM_000245.4:c.1771C>T