Allele Registry

Canonical Allele Identifier: PA645448230

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000437665

RCV000443188

ClinVar Variation:

376200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Tyr1253Asp	CA16602655 NM_001127500.3:c.3757T>G