Canonical Allele Identifier: PA238354
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 192101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Phe232Tyr
CA238352
NM_014000.2:c.695T>A