Canonical Allele Identifier: PA2828523948
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 21439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361425.1:p.Leu11Pro
CA342075
NM_001374496.1:c.32T>C