Allele Registry

Canonical Allele Identifier: PA2827254695

Gene: MET HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

50063

ClinVar RCV:

RCV000034529

RCV000121340

RCV000123120

RCV000163261

RCV000203290

RCV000421063

RCV000431770

RCV001507182

RCV002227927

RCV003891465

ClinVar Variation:

41624

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Thr562Ile	CA160417 NM_001324402.2:c.1685C>T