Canonical Allele Identifier: PA124771
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15121
ClinVar RCV Id: RCV000016278 RCV000016277 RCV001800300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Phe43del
CA124770
NM_000518.5:c.127_129del
CA217114487
NM_000518.5:c.126_128del