Canonical Allele Identifier: PA645445956
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_878899.1:p.Asn277Lys
CA2504195
NM_182896.3:c.831C>A
CA353678872
NM_182896.3:c.831C>G