Canonical Allele Identifier: PA2580124736
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2273425
ClinVar RCV Id: RCV002826402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000497.1:p.Arg314Ser
CA380266730
NM_000506.5:c.940C>A