Canonical Allele Identifier: PA2825104109
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2567662
ClinVar RCV Id: RCV003311353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Ser1236Arg
CA368991668
NM_000245.4:c.3706A>C
CA368991678
NM_000245.4:c.3708T>A
CA368991679
NM_000245.4:c.3708T>G