Allele Registry

Canonical Allele Identifier: PA125232

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016640

ClinVar Variation:

15387

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro6Arg	CA125231 NM_000518.5:c.17C>G