Canonical Allele Identifier: PA2580104905
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703827
ClinVar RCV Id: RCV002280986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Leu264Trp
CA358937076
NM_000128.4:c.791T>G