Canonical Allele Identifier: PA124781
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15126
ClinVar RCV Id: RCV000016284 RCV000016285 RCV000202507 RCV000224028 RCV000576347 RCV001535943 RCV001813746 RCV002415418 RCV002288494 RCV003335041 RCV003137529 RCV003150807 RCV004017254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu7Lys
CA124780
NM_000518.5:c.19G>A