Allele Registry

Canonical Allele Identifier: PA2826946887

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011328

ClinVar Variation:

10582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Asn128Tyr	CA255337 NM_001313913.2:c.382A>T