Allele Registry

Canonical Allele Identifier: PA125626

Gene: HBA2 HGNC NCBI

ClinVar RCV:

RCV000016955

ClinVar Variation:

15669

HGVS (amino-acid)	Matching Registered Transcripts
NP_000508.1:p.Leu67Pro	CA125625 NM_000517.6:c.200T>C