Canonical Allele Identifier: PA313947
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 205157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Ala267Thr
CA313946
NM_017882.3:c.799G>A