Allele Registry

Canonical Allele Identifier: PA124850

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016341

RCV000030906

RCV000507382

ClinVar Variation:

15169

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp80Asn	CA124849 NM_000518.5:c.238G>A