Allele Registry

Canonical Allele Identifier: PA125932

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017183

ClinVar Variation:

15838

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Ala111Thr	CA125931 NM_000558.5:c.331G>A