Allele Registry

Canonical Allele Identifier: PA2580254873

Gene: AMBP HGNC NCBI

ClinVar RCV:

RCV004142638

ClinVar Variation:

2293581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001624.1:p.Glu276Gln	CA374586045 NM_001633.4:c.826G>C