Canonical Allele Identifier: PA099318
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15483
ClinVar RCV Id: RCV000016741 RCV000674175 RCV000756239 RCV001260263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val127Gly
CA125340
NM_000518.5:c.380T>G