Allele Registry

Canonical Allele Identifier: PA125882

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017152

ClinVar Variation:

15811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Lys57Glu	CA125881 NM_000558.5:c.169A>G