Canonical Allele Identifier: PA2741813788
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2587482
ClinVar RCV Id: RCV003360896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Ser990Arg
CA368987249
NM_000245.4:c.2968A>C
CA368987257
NM_000245.4:c.2970C>A
CA368987259
NM_000245.4:c.2970C>G