Canonical Allele Identifier: PA125238
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15390
ClinVar RCV Id: RCV000016643 RCV000641622
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.His98Leu
CA125237
NM_000518.5:c.293A>T