Canonical Allele Identifier: PA125087
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15300
ClinVar RCV Id: RCV000016533 RCV000641556 RCV000759801 RCV002496379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val21Met
CA125086
NM_000518.5:c.61G>A