Allele Registry

Canonical Allele Identifier: PA125481

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016845

RCV001029750

RCV003886362

ClinVar Variation:

15578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro37His	CA125480 NM_000518.5:c.110C>A