Canonical Allele Identifier: PA124821
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15150
ClinVar RCV Id: RCV000016313 RCV000506646 RCV001826463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Thr88Lys
CA124820
NM_000518.5:c.263C>A