Allele Registry

Canonical Allele Identifier: PA915958100

Gene: HBB HGNC NCBI

ClinVar Allele:

30583

ClinVar RCV:

RCV000016810

ClinVar Variation:

15544

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu32Arg	CA217114670 NM_000518.5:c.95T>G