Canonical Allele Identifier: PA124848
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15168
ClinVar RCV Id: RCV000016340 RCV001811151 RCV001831569 RCV002281709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.His78Tyr
CA124847
NM_000518.5:c.232C>T