Canonical Allele Identifier: PA915993920
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1993
ClinVar RCV Id: RCV000002070 RCV003330381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167622.1:p.Arg97Cys
CA252023
NM_001174151.2:c.289C>T