Canonical Allele Identifier: PA2573062949
Gene: HBA2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Ala89Gly
CA276415009
NM_000517.6:c.266C>G