Canonical Allele Identifier: PA102930
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68200
ClinVar RCV Id: RCV000059032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys255Tyr
CA219154
NM_000128.4:c.764G>A