Canonical Allele Identifier: PA284820
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 68097
ClinVar RCV Id: RCV000058913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Phe238Ile
CA284819
NM_017882.3:c.712T>A