Canonical Allele Identifier: PA2828523414
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 422148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361422.1:p.Gln168Arg
CA16620398
NM_001374493.1:c.503A>G