Canonical Allele Identifier: PA2826112296
Gene: ARL13B HGNC NCBI
ClinVar RCV:
RCV001894493
ClinVar Variation:
1359528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167621.1:p.Asp365Gly
CA353679489
NM_001174150.2:c.1094A>G