Canonical Allele Identifier: PA124798
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15138
ClinVar RCV Id: RCV000016301 RCV000709890 RCV000396079 RCV000587680 RCV001107023 RCV001535933 RCV000855646 RCV001004567 RCV001107022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Gly70Ser
CA124797
NM_000518.5:c.208G>A