Canonical Allele Identifier: PA136738
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45594
ClinVar RCV Id: RCV000038810 RCV000172736 RCV000208305 RCV000252819 RCV001084130 RCV001293168 RCV003964863
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Amino-acid Alleles

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