Canonical Allele Identifier: PA213891
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15234
ClinVar RCV Id: RCV000016432 RCV000506942 RCV001004351 RCV001794452 RCV003338382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Arg31Thr
CA213890
NM_000518.5:c.92G>C