Canonical Allele Identifier: PA125626
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15669
ClinVar RCV Id: RCV000016955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Leu67Pro
CA125625
NM_000517.6:c.200T>C