Canonical Allele Identifier: PA2827106025
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 287670
ClinVar RCV Id: RCV000726050 RCV001082926 RCV003940043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308257.1:p.Asn262Lys
CA2504195
NM_001321328.2:c.786C>A
CA353678872
NM_001321328.2:c.786C>G