Canonical Allele Identifier: PA125167
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Leu111Pro
CA125166
NM_000518.5:c.332T>C