Canonical Allele Identifier: PA2825347701
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 322834
ClinVar RCV Id: RCV000264244 RCV000322260 RCV000757141 RCV002522934 RCV003165863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Val32Ile
CA8291552
NM_001031681.3:c.94G>A