Canonical Allele Identifier: PA2826112163
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 218107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167621.1:p.Tyr86Cys
CA279880
NM_001174150.2:c.257A>G