Canonical Allele Identifier: PA2828523441
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 4455
ClinVar RCV Id: RCV000004708 RCV001193377 RCV001781181 RCV002512767 RCV003904807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361422.1:p.Gly192Arg
CA278067
NM_001374493.1:c.574G>A
CA397694169
NM_001374493.1:c.574G>C