Allele Registry

Canonical Allele Identifier: PA2827253652

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001058831

RCV002436632

RCV003153915

RCV003467796

ClinVar Variation:

853915

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Leu900Val	CA368985772 NM_001324401.3:c.2698C>G