Canonical Allele Identifier: PA255429
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10639
ClinVar RCV Id: RCV000011385 RCV001001418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Val374Phe
CA255427
NM_000133.4:c.1120G>T