Canonical Allele Identifier: PA125491
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Thr124Asn
CA125490
NM_000518.5:c.371C>A