Canonical Allele Identifier: PA125411
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15534
ClinVar RCV Id: RCV000016799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu122Ala
CA125410
NM_000518.5:c.365A>C