Allele Registry

Canonical Allele Identifier: PA124885

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016368

RCV000506216

ClinVar Variation:

15187

439157

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His117Gln	CA217112701 NM_000518.5:c.351T>G CA217112705 NM_000518.5:c.351T>A