Canonical Allele Identifier: PA125651
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15685
ClinVar RCV Id: RCV000016974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Ser134Arg
CA125650
NM_000517.6:c.402C>A
CA276415491
NM_000517.6:c.400A>C
CA276415497
NM_000517.6:c.402C>G