Canonical Allele Identifier: PA2580112496
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2008516
ClinVar RCV Id: RCV002828675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr992Ser
CA368987276
NM_000245.4:c.2974A>T
CA368987278
NM_000245.4:c.2975C>G