Canonical Allele Identifier: PA109286
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10584
ClinVar RCV Id: RCV001390295 RCV000011330
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Arg191Cys
CA255340
NM_000133.4:c.571C>T