Canonical Allele Identifier: PA136763
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45602
ClinVar RCV Id: RCV000038819 RCV000171847 RCV000619949 RCV000678764 RCV000727177 RCV000988386 RCV003227625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Leu955del
CA136761
NM_014000.2:c.2862_2864del