Allele Registry

Canonical Allele Identifier: PA125079

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016529

RCV003736540

ClinVar Variation:

15296

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His3Gln	CA125078 NM_000518.5:c.9T>A CA217115595 NM_000518.5:c.9T>G