Canonical Allele Identifier: PA2825051122
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 695909
ClinVar RCV Id: RCV000861920 RCV001081775 RCV001825712 RCV002265904 RCV002478952 RCV003965649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Arg3His
CA10529706
NM_000133.4:c.8G>A