Canonical Allele Identifier: PA915993922
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 266096
ClinVar RCV Id: RCV000256476 RCV001092355 RCV001859504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167622.1:p.Arg97His
CA2504099
NM_001174151.2:c.290G>A