Allele Registry

Canonical Allele Identifier: PA124962

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016423

RCV001811155

ClinVar Variation:

15226

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly70Asp	CA124961 NM_000518.5:c.209G>A