Allele Registry

Canonical Allele Identifier: PA255415

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011368

ClinVar Variation:

10622

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ala436Glu	CA255413 NM_000133.4:c.1307C>A