Canonical Allele Identifier: PA645449764
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 420346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Val38Ile
CA4599201
NM_018941.4:c.112G>A