Allele Registry

Canonical Allele Identifier: PA2825621251

Gene: MET HGNC NCBI

ClinVar Variation Id: 2587482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser1008Arg	CA368987249 NM_001127500.3:c.3022A>C CA368987257 NM_001127500.3:c.3024C>A CA368987259 NM_001127500.3:c.3024C>G