Allele Registry

Canonical Allele Identifier: PA125506

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016862

ClinVar Variation:

15595

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Cys113Phe	CA125505 NM_000518.5:c.338G>T