Allele Registry

Canonical Allele Identifier: PA125504

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016860

ClinVar Variation:

15593

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys9Asn	CA125503 NM_000518.5:c.27G>C CA379274955 NM_000518.5:c.27G>T