Allele Registry

Canonical Allele Identifier: PA110186

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001000160

ClinVar Variation:

810865

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ile454Thr	CA414447553 NM_000133.4:c.1361T>C