Allele Registry

Canonical Allele Identifier: PA125411

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016799

ClinVar Variation:

15534

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu122Ala	CA125410 NM_000518.5:c.365A>C