Allele Registry

Canonical Allele Identifier: PA125195

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016618

RCV000985740

ClinVar Variation:

15367

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly84Cys	CA125194 NM_000518.5:c.250G>T