Allele Registry

Canonical Allele Identifier: PA2827254692

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000476062

RCV001018130

RCV001312218

RCV001755706

RCV001788226

ClinVar Variation:

411918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Pro561Ser	CA4448619 NM_001324402.2:c.1681C>T