Allele Registry

Canonical Allele Identifier: PA124792

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016298

RCV000757360

RCV003155027

ClinVar Variation:

15135

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe46Ser	CA124791 NM_000518.5:c.137T>C