Allele Registry

Canonical Allele Identifier: PA125515

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016869

RCV003476901

ClinVar Variation:

15602

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ser50Cys	CA125514 NM_000518.5:c.149C>G