Allele Registry

Canonical Allele Identifier: PA125453

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016830

ClinVar Variation:

15564

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gln132His	CA125452 NM_000518.5:c.396G>C CA379273679 NM_000518.5:c.396G>T