Canonical Allele Identifier: PA2580229382
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703828
ClinVar RCV Id: RCV002280987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341733.1:p.Phe30Ser
CA358957865
NM_001354804.2:c.89T>C