Allele Registry

Canonical Allele Identifier: PA125085

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016532

ClinVar Variation:

15299

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala87Asp	CA125084 NM_000518.5:c.260C>A