Canonical Allele Identifier: PA278483
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 189020
ClinVar RCV Id: RCV000169407 RCV001849327
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004928.2:p.Ser270del
CA278481
NM_004937.3:c.809_811del