Allele Registry

Canonical Allele Identifier: PA124948

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016415

ClinVar Variation:

15219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn58Asp	CA124947 NM_000518.5:c.172A>G