Canonical Allele Identifier: PA916014687
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56263
ClinVar RCV Id: RCV000049675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273033.1:p.Leu77Pro
CA263656
NM_001286104.2:c.230T>C