Allele Registry

Canonical Allele Identifier: PA124503

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016101

ClinVar Variation:

14961

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Lys66Asn	CA124502 NM_000184.3:c.198G>C CA217121305 NM_000184.3:c.198G>T