Allele Registry

Canonical Allele Identifier: PA2826947036

Gene: F9 HGNC NCBI

ClinVar Allele:

25647

ClinVar RCV:

RCV000011354

RCV003764551

ClinVar Variation:

10608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Val315Ala	CA255383 NM_001313913.2:c.944T>C