Canonical Allele Identifier: PA2828524069
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 422148
ClinVar RCV Id: RCV000479734 RCV000675105
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361425.1:p.Gln168Arg
CA16620398
NM_001374496.1:c.503A>G