Canonical Allele Identifier: PA2829812205
Gene: VPS13A HGNC NCBI

Linked Data

ClinVar Variation Id: 448864
ClinVar RCV Id: RCV000517261 RCV000605550 RCV001580041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056001.1:p.Tyr1587Cys
CA5092598
NM_015186.4:c.4760A>G