Allele Registry

Canonical Allele Identifier: PA109697

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011388

RCV001000171

ClinVar Variation:

10642

810871

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Cys396Ser	CA255433 NM_000133.4:c.1187G>C CA414446364 NM_000133.4:c.1186T>A