Allele Registry

Canonical Allele Identifier: PA124557

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016131

ClinVar Variation:

14991

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Trp16Arg	CA124556 NM_000184.3:c.46T>C CA379265221 NM_000184.3:c.46T>A