Canonical Allele Identifier: PA125562
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Leu110Arg
CA125561
NM_000517.6:c.329T>G