Canonical Allele Identifier: PA136754
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45599
ClinVar RCV Id: RCV000038816 RCV000126282 RCV000242411 RCV000458558 RCV000769116 RCV000709873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Ala934Val
CA136752
NM_014000.2:c.2801C>T