Canonical Allele Identifier: PA124913
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15201
ClinVar RCV Id: RCV000016384 RCV000759797 RCV001507092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val127Glu
CA124912
NM_000518.5:c.380T>A