Canonical Allele Identifier: PA2825347830
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 1511707
ClinVar RCV Id: RCV002548196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Ile123Val
CA8291700
NM_001031681.3:c.367A>G