Allele Registry

Canonical Allele Identifier: PA124745

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016262

ClinVar Variation:

15108

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu89Arg	CA124744 NM_000518.5:c.266T>G