Canonical Allele Identifier: PA125413
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15535
ClinVar RCV Id: RCV000016800 RCV000759071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val12Phe
CA125412
NM_000518.5:c.34G>T