Canonical Allele Identifier: PA104289
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2803
ClinVar RCV Id: RCV000002937 RCV001090293 RCV001851598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Trp263Cys
CA252416
NM_018941.4:c.789G>C
CA369954328
NM_018941.4:c.789G>T