Allele Registry

Canonical Allele Identifier: PA3057575689

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001265100

ClinVar Variation:

973814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Asn257_Arg260del	CA1139667802 NM_001313913.2:c.770_781del