Canonical Allele Identifier: PA342878
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 36337
ClinVar RCV Id: RCV000030006 RCV000506003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Arg31Lys
CA342877
NM_000518.5:c.92G>A