Canonical Allele Identifier: PA124889
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15189
ClinVar RCV Id: RCV000016370 RCV000756241 RCV001104053 RCV001107684 RCV001107685 RCV001107686 RCV001778655 RCV002482873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val12Ile
CA124888
NM_000518.5:c.34G>A