Canonical Allele Identifier: PA2828523948
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 21439
ClinVar RCV Id: RCV000020624 RCV001276660 RCV001781295 RCV002243657 RCV002513140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361425.1:p.Leu11Pro
CA342075
NM_001374496.1:c.32T>C