Canonical Allele Identifier: PA915958732
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 828138
ClinVar RCV Id: RCV001028011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Glu285Asp
CA414444506
NM_000133.4:c.855G>C
CA414444507
NM_000133.4:c.855G>T