Canonical Allele Identifier: PA109449
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10573
ClinVar RCV Id: RCV000011319 RCV000757260 RCV000852079 RCV001851790 RCV002490353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Arg75Gln
CA255318
NM_000133.4:c.224G>A