Allele Registry

Canonical Allele Identifier: PA916027585

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014903

RCV000419338

RCV000427546

RCV000438241

ClinVar Variation:

13889

376201

376202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Met820Ile	CA123611 NM_001324402.2:c.2460G>A CA16602656 NM_001324402.2:c.2460G>C CA16602657 NM_001324402.2:c.2460G>T