Canonical Allele Identifier: PA2573271370
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427758
ClinVar RCV Id: RCV001964685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Trp104Cys
CA369953298
NM_018941.4:c.312G>T
CA369953299
NM_018941.4:c.312G>C