Allele Registry

Canonical Allele Identifier: PA109647

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011345

ClinVar Variation:

10599

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Cys268Trp	CA255363 NM_000133.4:c.804T>G