Canonical Allele Identifier: PA252020
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1991
ClinVar RCV Id: RCV000002068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Arg79Gln
CA252019
NM_182896.3:c.236G>A