Canonical Allele Identifier: PA2741901427
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 2606641
ClinVar RCV Id: RCV004348935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Gly19Ser
CA5426340
NM_003380.5:c.55G>A