Allele Registry

Canonical Allele Identifier: PA255404

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011362

ClinVar Variation:

10616

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Met394Val	CA255402 NM_000133.4:c.1180A>G