Canonical Allele Identifier: PA102132
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 205180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Gly17Ser
CA313987
NM_017882.3:c.49G>A