Canonical Allele Identifier: PA645509872
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 439140
ClinVar RCV Id: RCV000507448 RCV000780324 RCV001078261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Met1Val