Canonical Allele Identifier: PA125099
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15309
ClinVar RCV Id: RCV000016549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val112Phe
CA125098
NM_000518.5:c.334G>T