Canonical Allele Identifier: PA1139729379
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 991257
ClinVar RCV Id: RCV001279439 RCV001871568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ile13Val
CA369952753
NM_018941.4:c.37A>G