Canonical Allele Identifier: PA916027564
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13882
ClinVar RCV Id: RCV000014896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val758Leu
CA256994
NM_001324402.2:c.2272G>T
CA368990990
NM_001324402.2:c.2272G>C