Canonical Allele Identifier: PA645445936
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 419776
ClinVar RCV Id: RCV000487423 RCV001052046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Ala36Thr
CA2503760
NM_182896.3:c.106G>A