Allele Registry

Canonical Allele Identifier: PA2826947147

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001382696

RCV004577675

ClinVar Variation:

1070514

3242390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Trp415Ter	CA2695236423 NM_001313913.2:c.1245del