Canonical Allele Identifier: PA125121
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15322
ClinVar RCV Id: RCV000016562 RCV000641598 RCV001284491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Tyr146Cys
CA125120
NM_000518.5:c.437A>G