Canonical Allele Identifier: PA2828523878
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 2012992
ClinVar RCV Id: RCV002856373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361424.1:p.Leu157Pro
CA397693145
NM_001374495.1:c.470T>C