Canonical Allele Identifier: PA2499238471
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1061371
ClinVar RCV Id: RCV001370941 RCV002465868 RCV002447489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Gly780Asp
CA368982027
NM_001127500.3:c.2339G>A