Allele Registry

Canonical Allele Identifier: PA2827254042

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002589570

RCV003871538

ClinVar Variation:

1911045

3017419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Tyr219His	CA368979474 NM_001324402.2:c.655T>C CA2740097508 NM_001324402.2:c.654_655delinsGC