Allele Registry

Canonical Allele Identifier: PA278478

Gene: CTNS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

34290

186970

ClinVar RCV:

RCV000020623

RCV000169266

RCV000780201

RCV002051792

RCV002513139

ClinVar Variation:

21438

188906

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026851.2:p.Ile67_Pro73del	CA278477 NM_001031681.3:c.199_219del CA342073 NM_001031681.3:c.198_218del