Canonical Allele Identifier: PA645476707
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 437255
ClinVar RCV Id: RCV000499478 RCV000765981 RCV002524332 RCV003902801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ala1006Gly
CA4823133
NM_152564.5:c.3017C>G