Allele Registry

Canonical Allele Identifier: PA2825620323

Gene: MET HGNC NCBI

ClinVar Variation Id: 1199923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser755Arg	CA164894406 NM_001127500.3:c.2263A>C CA368981471 NM_001127500.3:c.2265T>A CA368981473 NM_001127500.3:c.2265T>G