Canonical Allele Identifier: PA125089
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15302
ClinVar RCV Id: RCV000016537 RCV000029964 RCV001811161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Asp53Asn
CA125088
NM_000518.5:c.157G>A