Canonical Allele Identifier: PA2827254679
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1016629
ClinVar RCV Id: RCV001315660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val554Ile
CA368987170
NM_001324402.2:c.1660G>A