Canonical Allele Identifier: PA2826706673
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 418136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273039.1:p.Thr26Ser
CA7981009
NM_001286110.2:c.76A>T