Canonical Allele Identifier: PA125093
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val24Phe
CA125092
NM_000518.5:c.70G>T