Allele Registry

Canonical Allele Identifier: PA124964

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016425

ClinVar Variation:

15227

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys66Asn	CA124963 NM_000518.5:c.198G>C CA217114114 NM_000518.5:c.198G>T