Canonical Allele Identifier: PA110495
Gene: F9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Trp453Arg
CA255422
NM_000133.4:c.1357T>C
CA414447520
NM_000133.4:c.1357T>A