Allele Registry

Canonical Allele Identifier: PA125053

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016513

ClinVar Variation:

15283

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His98Pro	CA125052 NM_000518.5:c.293A>C