Allele Registry

Canonical Allele Identifier: PA125017

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016482

RCV000641527

RCV000985742

RCV005234182

ClinVar Variation:

15259

801186

3766487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His98Gln	CA217113533 NM_000518.5:c.294C>A CA217113536 NM_000518.5:c.294C>G