Canonical Allele Identifier: PA267598
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 100736
ClinVar RCV Id: RCV000087102 RCV000988030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn264Lys
CA267596
NM_018941.4:c.792C>G
CA369954335
NM_018941.4:c.792C>A