Canonical Allele Identifier: PA2826947038
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1417984
ClinVar RCV Id: RCV001930794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Ser316Arg
CA414445627
NM_001313913.2:c.946A>C
CA414445642
NM_001313913.2:c.948T>A
CA414445645
NM_001313913.2:c.948T>G