Canonical Allele Identifier: PA2825206145
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 3235090
ClinVar RCV Id: RCV004547426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ala129Thr
CA5839695
NM_000518.5:c.385G>A