Canonical Allele Identifier: PA2826946907
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10584
ClinVar RCV Id: RCV001390295 RCV000011330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Arg153Cys
CA255340
NM_001313913.2:c.457C>T