Canonical Allele Identifier: PA2827105886
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 218107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308257.1:p.Tyr71Cys
CA279880
NM_001321328.2:c.212A>G