Canonical Allele Identifier: PA125059
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15286
ClinVar RCV Id: RCV000016516 RCV001284155
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val114Glu
CA125058
NM_000518.5:c.341T>A