Canonical Allele Identifier: PA099297
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15333
ClinVar RCV Id: RCV000016573 RCV000016574 RCV000016575 RCV000224000 RCV000477892 RCV000623118 RCV000576548 RCV000723337 RCV001192494 RCV001255121 RCV001535873 RCV002251908 RCV002288496 RCV001824571 RCV003150808 RCV003989286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu7Val
CA125138
NM_000518.5:c.20A>T