Allele Registry

Canonical Allele Identifier: PA2825103616

Gene: MET HGNC NCBI

ClinVar Variation Id: 2567671

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Ser966Arg	CA368986937 NM_000245.4:c.2896A>C CA368986949 NM_000245.4:c.2898T>A CA368986950 NM_000245.4:c.2898T>G