Canonical Allele Identifier: PA264187
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56716
ClinVar RCV Id: RCV000050129
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Trp213del
CA264185
NM_018941.4:c.637_639del