Allele Registry

Canonical Allele Identifier: PA125014

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016478

ClinVar Variation:

15257

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala116Pro	CA125013 NM_000518.5:c.346G>C