Allele Registry

Canonical Allele Identifier: PA124497

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016098

ClinVar Variation:

14958

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Asp8Asn	CA124496 NM_000184.3:c.22G>A