Canonical Allele Identifier: PA125655
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Gly60Arg
CA125654
NM_000517.6:c.178G>C