Canonical Allele Identifier: PA2827254288
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 960489
ClinVar RCV Id: RCV001234021 RCV003166440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Phe356Ser
CA368982564
NM_001324402.2:c.1067T>C