Allele Registry

Canonical Allele Identifier: PA2826946968

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011345

ClinVar Variation:

10599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Cys230Trp	CA255363 NM_001313913.2:c.690T>G