Allele Registry

Canonical Allele Identifier: PA2741811734

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV003388353

ClinVar Variation:

2627159

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Pro324His	CA414445085 NM_000133.4:c.971C>A