Canonical Allele Identifier: PA2825048835
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091393
ClinVar RCV Id: RCV004385779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Asp307Val
CA3163817
NM_000128.4:c.920A>T