Canonical Allele Identifier: PA125047
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15278
ClinVar RCV Id: RCV000016504 RCV000016505 RCV000016506 RCV000016507 RCV000016508 RCV000506157 RCV000755549 RCV001835628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Lys96Glu
CA036550
NM_000518.5:c.[286A>G;19G>A]
CA125046
NM_000518.5:c.286A>G