Canonical Allele Identifier: PA2826947043
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10611
ClinVar RCV Id: RCV000011357 RCV000851648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Gly319Arg
CA255389
NM_001313913.2:c.955G>A
CA414445690
NM_001313913.2:c.955G>C