Allele Registry

Canonical Allele Identifier: PA110553

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011340

ClinVar Variation:

10594

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val228Leu	CA121130 NM_000133.4:c.682G>C