Allele Registry

Canonical Allele Identifier: PA125394

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016788

ClinVar Variation:

15524

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe104Ile	CA125393 NM_000518.5:c.310T>A