Allele Registry

Canonical Allele Identifier: PA2826929051

Gene: AMPD2 HGNC NCBI

ClinVar RCV:

RCV000119279

ClinVar Variation:

132810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295099.1:p.Glu703Asp	CA156214 NM_001308170.1:c.2109G>C CA341562802 NM_001308170.1:c.2109G>T