Allele Registry

Canonical Allele Identifier: PA2826947015

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV002512419

ClinVar Variation:

1879774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Leu289Pro	CA414445178 NM_001313913.2:c.866T>C