Canonical Allele Identifier: PA2829891174
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1440587
ClinVar RCV Id: RCV001967704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Gln1009Leu
CA371865760
NM_017890.5:c.3026A>T