Allele Registry

Canonical Allele Identifier: PA916027607

Gene: MET HGNC NCBI

ClinVar Allele:

522773

ClinVar RCV:

RCV000628769

RCV000765921

RCV001021839

RCV001766335

RCV002268220

RCV003459489

ClinVar Variation:

524889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Ile915Thr	CA4448820 NM_001324402.2:c.2744T>C