Canonical Allele Identifier: PA2573229422
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 1353044
ClinVar RCV Id: RCV002040136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Arg45His
CA5426356
NM_003380.5:c.134G>A