Canonical Allele Identifier: PA1139729446
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 991258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Arg54Cys
CA4599219
NM_018941.4:c.160C>T