Allele Registry

Canonical Allele Identifier: PA2580105491

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV002512419

ClinVar Variation:

1879774

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Leu327Pro	CA414445178 NM_000133.4:c.980T>C