Allele Registry

Canonical Allele Identifier: PA125617

Gene: HBA2 HGNC NCBI

ClinVar RCV:

RCV000016950

ClinVar Variation:

15664

HGVS (amino-acid)	Matching Registered Transcripts
NP_000508.1:p.His59Gln	CA125616 NM_000517.6:c.177C>A CA393993470 NM_000517.6:c.177C>G