Canonical Allele Identifier: PA342078
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 21440
ClinVar RCV Id: RCV000020625 RCV000590697 RCV002513141 RCV003105775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Asp205Asn
CA342077
NM_001031681.3:c.613G>A