Allele Registry

Canonical Allele Identifier: PA125517

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016870

ClinVar Variation:

15603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys62Gln	CA125516 NM_000518.5:c.184A>C