Allele Registry

Canonical Allele Identifier: PA125533

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016881

ClinVar Variation:

15614

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu27Ala	CA125532 NM_000518.5:c.80A>C