Canonical Allele Identifier: PA2829451509
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 3188561
ClinVar RCV Id: RCV004482456
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Ser72Arg
CA376175513
NM_003380.5:c.214A>C
CA376175527
NM_003380.5:c.216C>A
CA376175528
NM_003380.5:c.216C>G