Allele Registry

Canonical Allele Identifier: PA2826946985

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV003066389

ClinVar Variation:

2138741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg256Leu	CA414444639 NM_001313913.2:c.767G>T