Canonical Allele Identifier: PA915958789
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 810869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Asn392Asp
CA414446319
NM_000133.4:c.1174A>G