Canonical Allele Identifier: PA110010
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10647
ClinVar RCV Id: RCV000011393 RCV001810851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly357Glu
CA255437
NM_000133.4:c.1070G>A