Canonical Allele Identifier: PA645445949
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 266096
ClinVar RCV Id: RCV000256476 RCV001092355 RCV001859504
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Arg200His
CA2504099
NM_182896.3:c.599G>A