Canonical Allele Identifier: PA2828215310
Gene: CLN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 527752
ClinVar RCV Id: RCV000632713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353553.1:p.Phe167Ser
CA388309412
NM_001366624.2:c.500T>C