Canonical Allele Identifier: PA125012
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15256
ClinVar RCV Id: RCV000016466 RCV000641524 RCV000988480 RCV001266995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.His64Tyr
CA125011
NM_000518.5:c.190C>T