Canonical Allele Identifier: PA645476920
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 427100
ClinVar RCV Id: RCV000489122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser1812Ile
CA371872385
NM_017890.5:c.5435G>T