Canonical Allele Identifier: PA2826112432
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1359528
ClinVar RCV Id: RCV001894493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167622.1:p.Asp262Gly
CA353679489
NM_001174151.2:c.785A>G