Allele Registry

Canonical Allele Identifier: PA124982

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016438

RCV000780333

ClinVar Variation:

15238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro125Arg	CA124981 NM_000518.5:c.374C>G