Allele Registry

Canonical Allele Identifier: PA124990

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016448

ClinVar Variation:

15243

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu7Gln	CA124989 NM_000518.5:c.19G>C