Canonical Allele Identifier: PA263680
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56273
ClinVar RCV Id: RCV000049685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035897.1:p.Ala158Pro
CA263676
NM_001042432.2:c.472G>C