Allele Registry

Canonical Allele Identifier: PA255429

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011385

RCV001001418

ClinVar Variation:

10639

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val374Phe	CA255427 NM_000133.4:c.1120G>T