Canonical Allele Identifier: PA2827105879
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1991
ClinVar RCV Id: RCV000002068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308257.1:p.Arg64Gln
CA252019
NM_001321328.2:c.191G>A