Allele Registry

Canonical Allele Identifier: PA234268

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000153492

RCV001850098

RCV002354358

ClinVar Variation:

167293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Gly1288Ser	CA234266 NM_001127500.3:c.3862G>A