Canonical Allele Identifier: PA2580421384
Gene: VPS13D HGNC NCBI

Linked Data

ClinVar Variation Id: 1933113
ClinVar RCV Id: RCV002635790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060626.2:p.Ser84Thr
CA338475311
NM_018156.4:c.251G>C