Allele Registry

Canonical Allele Identifier: PA2741816108

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV003477269

ClinVar Variation:

2681977

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Trp38Cys	CA217114563 NM_000518.5:c.114G>T CA379274576 NM_000518.5:c.114G>C