Allele Registry

Canonical Allele Identifier: PA125437

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016819

ClinVar Variation:

15553

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala63Asp	CA125436 NM_000518.5:c.188C>A