Allele Registry

Canonical Allele Identifier: PA124810

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016307

RCV000641431

ClinVar Variation:

15144

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His147Leu	CA124809 NM_000518.5:c.440A>T