Canonical Allele Identifier: PA2830262666
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1359528
ClinVar RCV Id: RCV001894493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659433.2:p.Asp258Gly
CA353679489
NM_144996.4:c.773A>G