Allele Registry

Canonical Allele Identifier: PA3057319932

Gene: MET HGNC NCBI

ClinVar Allele:

3556809

ClinVar RCV:

RCV004944229

ClinVar Variation:

3395142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Trp481Arg	CA368986211 NM_001324402.2:c.1441T>A CA368986212 NM_001324402.2:c.1441T>C