Canonical Allele Identifier: PA125645
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15682
ClinVar RCV Id: RCV000016971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Lys140Asn
CA125644
NM_000517.6:c.420A>C
CA393994683
NM_000517.6:c.420A>T