Canonical Allele Identifier: PA915958084
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 626961
ClinVar RCV Id: RCV000851645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Ser120Gly
CA343141901
NM_000130.5:c.358A>G