Allele Registry

Canonical Allele Identifier: PA916021268

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000851938

ClinVar Variation:

627177

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ile98Thr	CA414438824 NM_001313913.2:c.293T>C