Canonical Allele Identifier: PA102965
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 11901
ClinVar RCV Id: RCV000012676 RCV000802420 RCV001273715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys56Arg
CA121763
NM_000128.4:c.166T>C