Allele Registry

Canonical Allele Identifier: PA2580105480

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV003066389

ClinVar Variation:

2138741

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Arg294Leu	CA414444639 NM_000133.4:c.881G>T