Allele Registry

Canonical Allele Identifier: PA125421

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016806

RCV000756240

RCV001826470

RCV002271370

ClinVar Variation:

15540

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro6Ser	CA125420 NM_000518.5:c.16C>T