Allele Registry

Canonical Allele Identifier: PA2741833487

Gene: MET HGNC NCBI

ClinVar Variation Id: 2766346

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser773Arg	CA368981888 NM_001127500.3:c.2317A>C CA368981904 NM_001127500.3:c.2319T>A CA368981911 NM_001127500.3:c.2319T>G