Canonical Allele Identifier: PA110391
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ser411Gly
CA255441
NM_000133.4:c.1231A>G
CA2695236388
NM_000133.4:c.1230_1231delinsCG