Allele Registry

Canonical Allele Identifier: PA125529

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016878

ClinVar Variation:

15611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala87Pro	CA125528 NM_000518.5:c.259G>C