Canonical Allele Identifier: PA103137
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 11895
ClinVar RCV Id: RCV000012670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Phe460Val
CA121750
NM_000128.4:c.1378T>G