Allele Registry

Canonical Allele Identifier: PA124573

Gene: HBG2 HGNC NCBI

ClinVar RCV:

RCV000016142

ClinVar Variation:

15002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000175.1:p.Phe119Leu	CA124572 NM_000184.3:c.355T>C CA379263632 NM_000184.3:c.357C>G CA379263633 NM_000184.3:c.357C>A