Allele Registry

Canonical Allele Identifier: PA125021

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016485

ClinVar Variation:

15261

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His3Pro	CA125020 NM_000518.5:c.8A>C