Allele Registry

Canonical Allele Identifier: PA124519

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016109

ClinVar Variation:

14969

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Gly2Cys	CA124518 NM_000184.3:c.4G>T