Canonical Allele Identifier: PA263699
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56277
ClinVar RCV Id: RCV000049689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035897.1:p.Leu170Pro
CA263696
NM_001042432.2:c.509T>C