Allele Registry

Canonical Allele Identifier: PA125465

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016837

ClinVar Variation:

15570

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu82His	CA125464 NM_000518.5:c.245T>A