Canonical Allele Identifier: PA1139709005
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 930366
ClinVar RCV Id: RCV001195968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Arg381Cys
CA5426688
NM_003380.5:c.1141C>T