Allele Registry

Canonical Allele Identifier: PA125613

Gene: HBA2 HGNC NCBI

ClinVar RCV:

RCV000016948

RCV001284150

ClinVar Variation:

15662

HGVS (amino-acid)	Matching Registered Transcripts
NP_000508.1:p.Asp127Asn	CA125612 NM_000517.6:c.379G>A