Canonical Allele Identifier: PA2829448953
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 1063922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003364.1:p.Asn163Asp
CA377266817
NM_003373.4:c.487A>G