Allele Registry

Canonical Allele Identifier: PA125471

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016840

ClinVar Variation:

15573

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn140Thr	CA125470 NM_000518.5:c.419A>C