Allele Registry

Canonical Allele Identifier: PA125497

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016855

RCV000588829

RCV000855596

RCV001835629

ClinVar Variation:

15588

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val135Ala	CA125496 NM_000518.5:c.404T>C