Canonical Allele Identifier: PA104241
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56707
ClinVar RCV Id: RCV000050120 RCV002513703
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.His139Tyr
CA264165
NM_018941.4:c.415C>T