Allele Registry

Canonical Allele Identifier: PA124806

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016305

ClinVar Variation:

15142

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp22Gly	CA124805 NM_000518.5:c.65A>G