Canonical Allele Identifier: PA136738
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.His636Arg
CA136736
NM_014000.2:c.1907A>G