Canonical Allele Identifier: PA124721
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15094
ClinVar RCV Id: RCV000016247 RCV000641405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Glu102Gly
CA124720
NM_000518.5:c.305A>G