Allele Registry

Canonical Allele Identifier: PA125037

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016497

RCV003447476

ClinVar Variation:

15271

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu69Pro	CA125036 NM_000518.5:c.206T>C