Canonical Allele Identifier: PA124868
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15178
ClinVar RCV Id: RCV000016356 RCV000756231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu23Gly
CA124867
NM_000518.5:c.68A>G