Allele Registry

Canonical Allele Identifier: PA124733

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016256

RCV001272128

RCV001281733

RCV002490848

ClinVar Variation:

15102

439134

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Arg41Ser	CA124732 NM_000518.5:c.123G>C CA217114512 NM_000518.5:c.123G>T