Canonical Allele Identifier: PA2580366062
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 2034328
ClinVar RCV Id: RCV002885421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Ser958Phe
CA377264782
NM_014000.2:c.2873C>T