Canonical Allele Identifier: PA241755
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 195345
ClinVar RCV Id: RCV000632691 RCV000724133 RCV001273351 RCV001838985 RCV002317017 RCV003224189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala67Val
CA241753
NM_018941.4:c.200C>T