Canonical Allele Identifier: PA1139730538
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 968370
ClinVar RCV Id: RCV001243486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Ala936Pro
CA377264639
NM_014000.2:c.2806G>C