Canonical Allele Identifier: PA136819
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45623
ClinVar RCV Id: RCV000038842 RCV000472922 RCV002483002 RCV003372609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Arg318Cys
CA136817
NM_014000.2:c.952C>T