Canonical Allele Identifier: PA2825103219
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1789782
ClinVar RCV Id: RCV002448237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr761Ile
CA368982003
NM_000245.4:c.2282C>T