Canonical Allele Identifier: PA279881
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 218107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Tyr86Cys
CA279880
NM_182896.3:c.257A>G