Canonical Allele Identifier: PA314057
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 205208
ClinVar RCV Id: RCV000556468 RCV000187143 RCV001273353 RCV002321751
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Val136Phe
CA314055
NM_018941.4:c.406G>T