Canonical Allele Identifier: PA125439
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15554
ClinVar RCV Id: RCV000016820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu27Gly
CA125438
NM_000518.5:c.80A>G