Allele Registry

Canonical Allele Identifier: PA916027586

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000425451

RCV000442904

RCV003168614

ClinVar Variation:

376126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Met820Thr	CA16602584 NM_001324402.2:c.2459T>C