Allele Registry

Canonical Allele Identifier: PA2828290541

Gene: AMPD2 HGNC NCBI

ClinVar RCV:

RCV000119279

ClinVar Variation:

132810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355738.1:p.Glu724Asp	CA156214 NM_001368809.2:c.2172G>C CA341562802 NM_001368809.2:c.2172G>T