Canonical Allele Identifier: PA915993910
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 217552
ClinVar RCV Id: RCV000201595 RCV002282036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167622.1:p.Asn51Ser
CA277722
NM_001174151.2:c.152A>G