Allele Registry

Canonical Allele Identifier: PA125061

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016518

ClinVar Variation:

15287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His93Pro	CA125060 NM_000518.5:c.278A>C