Allele Registry

Canonical Allele Identifier: PA125081

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016530

ClinVar Variation:

15297

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Cys94Arg	CA125080 NM_000518.5:c.280T>C