Canonical Allele Identifier: PA124765
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu102Lys
CA124764
NM_000518.5:c.304G>A