Canonical Allele Identifier: PA2827254668
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 856076
ClinVar RCV Id: RCV001061469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr547Ile
CA368987081
NM_001324402.2:c.1640C>T