Allele Registry

Canonical Allele Identifier: PA2826946993

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011349

RCV001001417

RCV002512971

ClinVar Variation:

10603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg260Ter