Canonical Allele Identifier: PA264193
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56719
ClinVar RCV Id: RCV000050132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gln256Glu
CA264191
NM_018941.4:c.766C>G