Allele Registry

Canonical Allele Identifier: PA125373

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016771

ClinVar Variation:

15509

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu32Val	CA125372 NM_000518.5:c.94C>G