Canonical Allele Identifier: PA1139729675
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 855190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Met200Val
CA4599317
NM_018941.4:c.598A>G