Canonical Allele Identifier: PA125041
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15274
ClinVar RCV Id: RCV000016500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.His98Tyr
CA125040
NM_000518.5:c.292C>T