Allele Registry

Canonical Allele Identifier: PA125782

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017068

RCV000017069

ClinVar Variation:

15758

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Ala13Asp	CA125781 NM_000558.5:c.38C>A