Canonical Allele Identifier: PA136705
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45582
ClinVar RCV Id: RCV000157581 RCV000172735 RCV000253868 RCV000624752 RCV001081141 RCV000852616 RCV000038798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Ile519Leu
CA136703
NM_014000.2:c.1555A>C