Allele Registry

Canonical Allele Identifier: PA125386

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016784

ClinVar Variation:

15520

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp22His	CA125385 NM_000518.5:c.64G>C