Allele Registry

Canonical Allele Identifier: PA124980

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016437

ClinVar Variation:

15237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly70Arg	CA124979 NM_000518.5:c.208G>C