Canonical Allele Identifier: PA124815
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15147
ClinVar RCV Id: RCV000016310 RCV000641434 RCV001374642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ser90Asn
CA124814
NM_000518.5:c.269G>A