Allele Registry

Canonical Allele Identifier: PA125349

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016749

RCV000029973

RCV000508492

RCV002504798

ClinVar Variation:

15489

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr88Pro	CA125348 NM_000518.5:c.262A>C