Canonical Allele Identifier: PA645477129
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 437248
ClinVar RCV Id: RCV000502353 RCV002524330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Pro3969His
CA371795664
NM_017890.5:c.11906C>A