Canonical Allele Identifier: PA125002
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15251
ClinVar RCV Id: RCV000016458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Phe43Leu
CA125001
NM_000518.5:c.127T>C
CA379274520
NM_000518.5:c.129T>A
CA379274522
NM_000518.5:c.129T>G