Canonical Allele Identifier: PA124998
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu8del
CA124997
NM_000518.5:c.22_24del