Canonical Allele Identifier: PA124878
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15183
ClinVar RCV Id: RCV000016362 RCV000016363 RCV001731302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Leu29Pro
CA124877
NM_000518.5:c.86T>C