Allele Registry

Canonical Allele Identifier: PA124862

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016352

RCV003234907

ClinVar Variation:

15175

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu7Ala	CA124861 NM_000518.5:c.20A>C