Allele Registry

Canonical Allele Identifier: PA125390

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016786

RCV001001454

ClinVar Variation:

15522

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp80His	CA125389 NM_000518.5:c.238G>C