Canonical Allele Identifier: PA125417
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15538
ClinVar RCV Id: RCV000016803 RCV000016804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Gly26del
CA125416
NM_000518.5:c.77_79del