Canonical Allele Identifier: PA658825441
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 553257
ClinVar RCV Id: RCV000668664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Gly573Glu
CA3164105
NM_000128.4:c.1718G>A