Allele Registry

Canonical Allele Identifier: PA124521

Gene: HBG2 HGNC NCBI

ClinVar Allele:

30009

ClinVar RCV:

RCV000016110

ClinVar Variation:

14970

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.His118Arg	CA124520 NM_000184.3:c.353A>G