Canonical Allele Identifier: PA2825348112
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 2012992
ClinVar RCV Id: RCV002856373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Leu304Pro
CA397693145
NM_001031681.3:c.911T>C