Canonical Allele Identifier: PA2826112308
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 346913
ClinVar RCV Id: RCV000764518 RCV001705515 RCV003912464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167621.1:p.Gly384Glu
CA2504290
NM_001174150.2:c.1151G>A