Allele Registry

Canonical Allele Identifier: PA658720280

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000587770

ClinVar Variation:

496002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val24Leu	CA379274808 NM_000518.5:c.70G>C