Canonical Allele Identifier: PA915958080
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 626955
ClinVar RCV Id: RCV000851635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Ser111Arg
CA343141986
NM_000130.5:c.333C>G
CA343141988
NM_000130.5:c.333C>A
CA343141994
NM_000130.5:c.331A>C