Canonical Allele Identifier: PA2829819717
Gene: VPS13D HGNC NCBI

Linked Data

ClinVar Variation Id: 1029392
ClinVar RCV Id: RCV001330664 RCV002546402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056193.2:p.Asn98Ser
CA601162
NM_015378.4:c.293A>G