Allele Registry

Canonical Allele Identifier: PA916066857

Gene: ALG13 HGNC NCBI

ClinVar Variation Id: 516978

HGVS (amino-acid)	Matching Registered Transcripts
NP_060936.1:p.Phe5Leu	CA10493417 NM_018466.6:c.13T>C CA414247972 NM_018466.6:c.15T>A CA414247973 NM_018466.6:c.15T>G