Canonical Allele Identifier: PA277010
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210736
ClinVar RCV Id: RCV000192707 RCV001580081 RCV002307439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.His157Arg
CA277008
NM_018941.4:c.470A>G