Allele Registry

Canonical Allele Identifier: PA126938

Gene: ALAD HGNC NCBI

ClinVar RCV:

RCV000018363

RCV000413492

ClinVar Variation:

16867

HGVS (amino-acid)	Matching Registered Transcripts
NP_000022.3:p.Phe12Leu	CA126937 NM_000031.6:c.36C>G CA374565903 NM_000031.6:c.36C>A CA374565913 NM_000031.6:c.34T>C