Canonical Allele Identifier: PA125566
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Gly16Asp
CA125565
NM_000517.6:c.47G>A