Canonical Allele Identifier: PA2573312438
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1359528
ClinVar RCV Id: RCV001894493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Asp365Gly
CA353679489
NM_182896.3:c.1094A>G