Canonical Allele Identifier: PA645449884
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 419577
ClinVar RCV Id: RCV000478132 RCV001833609 RCV002525804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Leu133Phe
CA16618618
NM_018941.4:c.399G>T
CA369953485
NM_018941.4:c.399G>C