Allele Registry

Canonical Allele Identifier: PA125475

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016842

ClinVar Variation:

15575

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro37Ala	CA125474 NM_000518.5:c.109C>G