Allele Registry

Canonical Allele Identifier: PA124978

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016436

RCV000641495

ClinVar Variation:

15236

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp100Asn	CA124977 NM_000518.5:c.298G>A