Canonical Allele Identifier: PA263628
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035897.1:p.Asp416Gly
CA263624
NM_001042432.2:c.1247A>G