Canonical Allele Identifier: PA2573271080
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1518374
ClinVar RCV Id: RCV002021699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Pro3986Ala
CA371795869
NM_017890.5:c.11956C>G