Canonical Allele Identifier: PA658830253
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 553032
ClinVar RCV Id: RCV000668402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Asn3954del
CA658821989
NM_017890.5:c.11861_11863del