Allele Registry

Canonical Allele Identifier: PA916027536

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000418101

ClinVar Variation:

376729

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Asn670Tyr	CA16603137 NM_001324402.2:c.2008A>T