Allele Registry

Canonical Allele Identifier: PA124887

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016369

ClinVar Variation:

15188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly57Arg	CA124886 NM_000518.5:c.169G>C