Allele Registry

Canonical Allele Identifier: PA2741886742

Gene: AMBP HGNC NCBI

ClinVar RCV:

RCV004308503

ClinVar Variation:

2533957

HGVS (amino-acid)	Matching Registered Transcripts
NP_001624.1:p.Gln30His	CA374589494 NM_001633.4:c.90A>T CA374589496 NM_001633.4:c.90A>C