Allele Registry

Canonical Allele Identifier: PA125972

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017207

RCV001811184

ClinVar Variation:

15861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Lys8Asn	CA125971 NM_000558.5:c.24G>C CA393994922 NM_000558.5:c.24G>T