Canonical Allele Identifier: PA2826947135
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 811512
ClinVar RCV Id: RCV001001426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Cys397Tyr
CA414447219
NM_001313913.2:c.1190G>A