Allele Registry

Canonical Allele Identifier: PA125537

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016885

ClinVar Variation:

15618

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val24Ala	CA125536 NM_000518.5:c.71T>C