Canonical Allele Identifier: PA2580104908
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703826
ClinVar RCV Id: RCV002280985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys380Arg
CA358941486
NM_000128.4:c.1138T>C