Canonical Allele Identifier: PA125224
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ser90Arg
CA125223
NM_000518.5:c.268A>C
CA379273796
NM_000518.5:c.270T>G
CA379273797
NM_000518.5:c.270T>A