Allele Registry

Canonical Allele Identifier: PA125382

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016782

ClinVar Variation:

15518

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His3Leu	CA125381 NM_000518.5:c.8A>T