Canonical Allele Identifier: PA1139669390
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15250
ClinVar RCV Id: RCV000641506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.His144Gln
CA217112242
NM_000518.5:c.432C>G
CA217112246
NM_000518.5:c.432C>A