Allele Registry

Canonical Allele Identifier: PA2741886752

Gene: AMBP HGNC NCBI

ClinVar RCV:

RCV004294734

ClinVar Variation:

2519771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001624.1:p.Arg334Thr	CA5199853 NM_001633.4:c.1001G>C