Canonical Allele Identifier: PA2829811290
Gene: VPS13A HGNC NCBI

Linked Data

ClinVar Variation Id: 4682
ClinVar RCV Id: RCV000004946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056001.1:p.Ile90Lys
CA253246
NM_015186.4:c.269T>A