Canonical Allele Identifier: PA125415
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Gln128Arg
CA125414
NM_000518.5:c.383A>G