Canonical Allele Identifier: PA916039419
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68181
ClinVar RCV Id: RCV000059013 RCV003447484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341733.1:p.Thr51Ile
CA219118
NM_001354804.2:c.152C>T