Allele Registry

Canonical Allele Identifier: PA2827253921

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000121353

RCV000206655

RCV000210762

RCV001293429

RCV001562214

RCV003945083

ClinVar Variation:

134654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Arg161Trp	CA332158 NM_001324402.2:c.481C>T