Canonical Allele Identifier: PA125398
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15527
ClinVar RCV Id: RCV000016792 RCV002466407
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val68Gly
CA125397
NM_000518.5:c.203T>G