Canonical Allele Identifier: PA109253
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 216926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ala279Thr
CA277507
NM_000133.4:c.835G>A