Allele Registry

Canonical Allele Identifier: PA124940

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016409

ClinVar Variation:

15215

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys66Gln	CA124939 NM_000518.5:c.196A>C