Canonical Allele Identifier: PA125882
Gene: HBA1 HGNC NCBI
ClinVar RCV:
RCV000017152
ClinVar Variation:
15811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000549.1:p.Lys57Glu
CA125881
NM_000558.5:c.169A>G