Canonical Allele Identifier: PA214749
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 12199
ClinVar RCV Id: RCV000012983 RCV000056967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Glu151Lys
CA214748
NM_003380.5:c.451G>A