Canonical Allele Identifier: PA125539
Gene: HBB HGNC NCBI
ClinVar RCV:
RCV000016886
ClinVar Variation:
15619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ser10Tyr
CA125538
NM_000518.5:c.29C>A