Allele Registry

Canonical Allele Identifier: PA125425

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016812

ClinVar Variation:

15546

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe46Cys	CA125424 NM_000518.5:c.137T>G