Allele Registry

Canonical Allele Identifier: PA110563

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011339

ClinVar Variation:

10593

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val228Phe	CA255355 NM_000133.4:c.682G>T