Allele Registry

Canonical Allele Identifier: PA2830275873

Gene: AMPD2 HGNC NCBI

ClinVar RCV:

RCV000119279

ClinVar Variation:

132810

HGVS (amino-acid)	Matching Registered Transcripts
NP_631895.1:p.Glu697Asp	CA156214 NM_139156.4:c.2091G>C CA341562802 NM_139156.4:c.2091G>T