Canonical Allele Identifier: PA2826946913
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1959260
ClinVar RCV Id: RCV002710164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Pro159Ser
CA336137425
NM_001313913.2:c.475C>T