Canonical Allele Identifier: PA110067
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 811513
ClinVar RCV Id: RCV001001427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly442Glu
CA414447349
NM_000133.4:c.1325G>A