Canonical Allele Identifier: PA2828523572
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146761
ClinVar RCV Id: RCV003076840 RCV004070410
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361423.1:p.Gly92Ser
CA8291868
NM_001374494.1:c.274G>A