Canonical Allele Identifier: PA263659
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56263
ClinVar RCV Id: RCV000049675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035897.1:p.Leu101Pro
CA263656
NM_001042432.2:c.302T>C