Canonical Allele Identifier: PA102047
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 457972
ClinVar RCV Id: RCV000551912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Arg149Cys
CA7630608
NM_017882.3:c.445C>T