Canonical Allele Identifier: PA123024
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13313
ClinVar RCV Id: RCV002468931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000497.1:p.Arg425His
CA123022
NM_000506.5:c.1274G>A