Canonical Allele Identifier: PA109729
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_000124.1:p.Cys435Tyr
CA414447219
NM_000133.4:c.1304G>A