Canonical Allele Identifier: PA645419802
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 418137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035897.1:p.Arg405Trp
CA7980640
NM_001042432.2:c.1213C>T