Canonical Allele Identifier: PA124915
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15202
ClinVar RCV Id: RCV000016385 RCV000029996 RCV001004558 RCV001284489 RCV002290955 RCV002321485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Gly137Asp
CA124914
NM_000518.5:c.410G>A