Allele Registry

Canonical Allele Identifier: PA125628

Gene: HBA2 HGNC NCBI

ClinVar RCV:

RCV000016956

ClinVar Variation:

15670

HGVS (amino-acid)	Matching Registered Transcripts
NP_000508.1:p.Val56Ala	CA125627 NM_000517.6:c.167T>C