Allele Registry

Canonical Allele Identifier: PA125692

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017002

ClinVar Variation:

15708

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Pro38_Thr39insGlu	CA125690 NM_000558.5:c.114_115insGAA