Allele Registry

Canonical Allele Identifier: PA2580254875

Gene: AMBP HGNC NCBI

ClinVar RCV:

RCV004165084

ClinVar Variation:

2323720

HGVS (amino-acid)	Matching Registered Transcripts
NP_001624.1:p.Gly341Asp	CA5199849 NM_001633.4:c.1022G>A