Allele Registry

Canonical Allele Identifier: PA125043

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016501

ClinVar Variation:

15275

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly25Asp	CA125042 NM_000518.5:c.74G>A