Canonical Allele Identifier: PA916039437
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 554924
ClinVar RCV Id: RCV000670640 RCV002531256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341733.1:p.Thr141Met
CA3163650
NM_001354804.2:c.422C>T