Canonical Allele Identifier: PA2829449041
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 192101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003364.1:p.Phe232Tyr
CA238352
NM_003373.4:c.695T>A