Canonical Allele Identifier: PA124930
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15210
ClinVar RCV Id: RCV000016397
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Lys18Asn
CA124929
NM_000518.5:c.54G>C
CA217115354
NM_000518.5:c.54G>T