Canonical Allele Identifier: PA645449838
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 393260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala96Val
CA4599241
NM_018941.4:c.287C>T