Canonical Allele Identifier: PA109507
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167621.1:p.Arg200Cys
CA252023
NM_001174150.2:c.598C>T