Canonical Allele Identifier: PA2499277373
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1063922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Asn163Asp
CA377266817
NM_014000.2:c.487A>G