Canonical Allele Identifier: PA2827254696
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2008516
ClinVar RCV Id: RCV002828675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr562Ser
CA368987276
NM_001324402.2:c.1684A>T
CA368987278
NM_001324402.2:c.1685C>G