Allele Registry

Canonical Allele Identifier: PA1139712500

Gene: CLN5 HGNC NCBI

ClinVar RCV:

RCV001241884

ClinVar Variation:

967064

HGVS (amino-acid)	Matching Registered Transcripts
NP_006484.2:p.Trp26Cys	CA7007119 NM_006493.4:c.78G>T CA388306491 NM_006493.4:c.78G>C