Allele Registry

Canonical Allele Identifier: PA125493

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016852

ClinVar Variation:

15585

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val134Ala	CA125492 NM_000518.5:c.401T>C