Canonical Allele Identifier: PA1139729491
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 839247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn101Lys
CA4599247
NM_018941.4:c.303C>G
CA369953274
NM_018941.4:c.303C>A