Canonical Allele Identifier: PA125388
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Gly84Arg
CA125387
NM_000518.5:c.250G>C