Canonical Allele Identifier: PA1139729911
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 915719
ClinVar RCV Id: RCV001170936
ClinVar Variation Id: 1384902
ClinVar RCV Id: RCV001902689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Lys162Asn
CA377266811
NM_014000.2:c.486G>C
CA377266813
NM_014000.2:c.486G>T