Canonical Allele Identifier: PA102861
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68199
ClinVar RCV Id: RCV000059031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Arg252Thr
CA219152
NM_000128.4:c.755G>C