Allele Registry

Canonical Allele Identifier: PA124563

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016134

RCV000030902

ClinVar Variation:

14994

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Ile76Thr	CA124562 NM_000184.3:c.227T>C