Allele Registry

Canonical Allele Identifier: PA125419

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016805

ClinVar Variation:

15539

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val21Glu	CA125418 NM_000518.5:c.62T>A