Allele Registry

Canonical Allele Identifier: PA124934

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016399

ClinVar Variation:

15212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly26Asp	CA124933 NM_000518.5:c.77G>A