Allele Registry

Canonical Allele Identifier: PA2580254864

Gene: AMBP HGNC NCBI

ClinVar RCV:

RCV004277471

ClinVar Variation:

2488089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001624.1:p.Arg2Lys	CA5200313 NM_001633.4:c.5G>A