Allele Registry

Canonical Allele Identifier: PA124919

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016388

RCV000641476

ClinVar Variation:

15204

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp100Gly	CA124918 NM_000518.5:c.299A>G