Canonical Allele Identifier: PA2830317691
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1012602
ClinVar RCV Id: RCV001310639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Met3698Thr
CA371790378
NM_152564.5:c.11093T>C