Canonical Allele Identifier: PA2830312577
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 969707
ClinVar RCV Id: RCV001245112 RCV003399009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Thr7Ser
CA371856017
NM_152564.5:c.19A>T
CA371856020
NM_152564.5:c.20C>G