Canonical Allele Identifier: PA263679
Gene: CLN3 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000077.1:p.Ala158Pro
CA263676
NM_000086.2:c.472G>C