Canonical Allele Identifier: PA2741816141
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 2681982
ClinVar RCV Id: RCV003477274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val68Leu
CA379273869
NM_000518.5:c.202G>T
CA379273870
NM_000518.5:c.202G>C