Allele Registry

Canonical Allele Identifier: PA2573162474

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001973941

ClinVar Variation:

1477908

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ala279Pro	CA414443714 NM_000133.4:c.835G>C