Canonical Allele Identifier: PA238908
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 193389
ClinVar RCV Id: RCV000187111 RCV000515438 RCV000766779 RCV001085594 RCV002313023 RCV003917602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060352.1:p.Ala18Val
CA238907
NM_017882.3:c.53C>T