Allele Registry

Canonical Allele Identifier: PA124757

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016269

ClinVar Variation:

15114

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys62Met	CA124756 NM_000518.5:c.185A>T