Allele Registry

Canonical Allele Identifier: PA124788

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016296

ClinVar Variation:

15133

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp95Gly	CA124787 NM_000518.5:c.284A>G