Canonical Allele Identifier: PA314010
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 205192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Met200Thr
CA314008
NM_018941.4:c.599T>C