Allele Registry

Canonical Allele Identifier: PA124533

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016116

ClinVar Variation:

14976

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Trp131Gly	CA124532 NM_000184.3:c.391T>G