Canonical Allele Identifier: PA2826947065
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10613
ClinVar RCV Id: RCV000011359 RCV000851995 RCV001000156 RCV001851792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Arg341Gln
CA255394
NM_001313913.2:c.1022G>A