Allele Registry

Canonical Allele Identifier: PA124719

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016246

ClinVar Variation:

15093

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn20Asp	CA124718 NM_000518.5:c.58A>G