Canonical Allele Identifier: PA314028
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 205198
ClinVar RCV Id: RCV000187132 RCV001037746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gln279His
CA314026
NM_018941.4:c.837G>T
CA369954432
NM_018941.4:c.837G>C