Canonical Allele Identifier: PA125051
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15281
ClinVar RCV Id: RCV000016511 RCV001269803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Lys9Glu
CA125050
NM_000518.5:c.25A>G