Canonical Allele Identifier: PA2825622287
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2567662
ClinVar RCV Id: RCV003311353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ser1254Arg
CA368991668
NM_001127500.3:c.3760A>C
CA368991678
NM_001127500.3:c.3762T>A
CA368991679
NM_001127500.3:c.3762T>G