Allele Registry

Canonical Allele Identifier: PA125031

Gene: HBB HGNC NCBI

ClinVar Allele:

30306

ClinVar RCV:

RCV000016491

RCV001811158

ClinVar Variation:

15267

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ser45Cys	CA125030 NM_000518.5:c.134C>G