Canonical Allele Identifier: PA2827254273
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 849997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Asn348Thr
CA368982413
NM_001324402.2:c.1043A>C