Canonical Allele Identifier: PA2826943687
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 626923
ClinVar RCV Id: RCV000851584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Cys360Arg
CA388793686
NM_001312674.2:c.1078T>C