Allele Registry

Canonical Allele Identifier: PA124970

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016428

RCV001284154

ClinVar Variation:

15230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val110Leu	CA124969 NM_000518.5:c.328G>C CA217112786 NM_000518.5:c.328G>T