Canonical Allele Identifier: PA313982
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 205177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Asp256Gly
CA313981
NM_017882.3:c.767A>G