Canonical Allele Identifier: PA107583
Gene: XK HGNC NCBI
ClinVar Allele:
24807
ClinVar RCV:
RCV000010422
ClinVar Variation:
9768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066569.1:p.Cys294Arg
CA254889
NM_021083.4:c.880T>C