Canonical Allele Identifier: PA658809670
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 541104
ClinVar RCV Id: RCV000651306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Ser56Tyr
CA5426364
NM_003380.5:c.167C>A