Canonical Allele Identifier: PA658720280
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 496002
ClinVar RCV Id: RCV000587770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val24Leu
CA379274808
NM_000518.5:c.70G>C