Allele Registry

Canonical Allele Identifier: PA916022081

Gene: ALAD HGNC NCBI

ClinVar RCV:

RCV000018363

RCV000413492

ClinVar Variation:

16867

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304674.1:p.Phe21Leu	CA126937 NM_001317745.2:c.63C>G CA374565903 NM_001317745.2:c.63C>A CA374565913 NM_001317745.2:c.61T>C