Canonical Allele Identifier: PA2825348122
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 422148
ClinVar RCV Id: RCV000479734 RCV000675105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Gln315Arg
CA16620398
NM_001031681.3:c.944A>G