Allele Registry

Canonical Allele Identifier: PA125892

Gene: HBA1 HGNC NCBI

ClinVar RCV:

RCV000017158

ClinVar Variation:

15816

HGVS (amino-acid)	Matching Registered Transcripts
NP_000549.1:p.Lys128Thr	CA125891 NM_000558.5:c.383A>C