Canonical Allele Identifier: PA2826112380
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 287670
ClinVar RCV Id: RCV000726050 RCV001082926 RCV003940043
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167622.1:p.Asn174Lys
CA2504195
NM_001174151.2:c.522C>A
CA353678872
NM_001174151.2:c.522C>G