Canonical Allele Identifier: PA2741901428
Gene: VIM HGNC NCBI
ClinVar RCV:
RCV003742422
ClinVar Variation:
2872982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Arg28Gly
CA376174915
NM_003380.5:c.82C>G