Canonical Allele Identifier: PA2828215299
Gene: CLN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 56542
ClinVar RCV Id: RCV000049955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353553.1:p.Trp158Ser
CA263907
NM_001366624.2:c.473G>C