Canonical Allele Identifier: PA2827254239
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2155877
ClinVar RCV Id: RCV003090779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr329Ile
CA368981973
NM_001324402.2:c.986C>T