Canonical Allele Identifier: PA1139731898
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 855811
ClinVar RCV Id: RCV001061151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser3970Asn
CA371795677
NM_017890.5:c.11909G>A