Canonical Allele Identifier: PA1139669349
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869317
ClinVar RCV Id: RCV001078379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Asn140Ter
CA916083173
NM_000518.5:c.417dup