Allele Registry

Canonical Allele Identifier: PA3057549585

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV005241157

ClinVar Variation:

3769491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Val336Ile	CA414446027 NM_001313913.2:c.1006G>A