Allele Registry

Canonical Allele Identifier: PA2826442332

Gene: AMPD2 HGNC NCBI

ClinVar RCV:

RCV000119279

ClinVar Variation:

132810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244290.1:p.Glu660Asp	CA156214 NM_001257361.2:c.1980G>C CA341562802 NM_001257361.2:c.1980G>T