Canonical Allele Identifier: PA2573073032
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 4446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361425.1:p.Gly22Asp
CA278065
NM_001374496.1:c.65G>A