Canonical Allele Identifier: PA109512
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1991
ClinVar RCV Id: RCV000002068
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167621.1:p.Arg79Gln
CA252019
NM_001174150.2:c.236G>A