Canonical Allele Identifier: PA124891
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15190
ClinVar RCV Id: RCV000016371 RCV000016372 RCV000016373 RCV000757359 RCV001831570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Phe43Ser
CA124890
NM_000518.5:c.128T>C