Allele Registry

Canonical Allele Identifier: PA2825103209

Gene: MET HGNC NCBI

ClinVar Variation Id: 1199923

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Ser755Arg	CA164894406 NM_000245.4:c.2263A>C CA368981904 NM_000245.4:c.2265T>A CA368981911 NM_000245.4:c.2265T>G