Allele Registry

Canonical Allele Identifier: PA915966567

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000476062

RCV001018130

RCV001312218

RCV001755706

RCV001788226

ClinVar Variation:

411918

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Pro991Ser	CA4448619 NM_000245.4:c.2971C>T