Allele Registry

Canonical Allele Identifier: PA125435

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016818

ClinVar Variation:

15552

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys83Gln	CA125434 NM_000518.5:c.247A>C