Allele Registry

Canonical Allele Identifier: PA124749

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016264

RCV000016265

ClinVar Variation:

15110

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu122Val	CA124748 NM_000518.5:c.365A>T