Canonical Allele Identifier: PA204181
Gene: ARL13B HGNC NCBI

Linked Data

ClinVar Variation Id: 207910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878899.1:p.Val127Leu
CA204179
NM_182896.3:c.379G>T
CA353675847
NM_182896.3:c.379G>C