Allele Registry

Canonical Allele Identifier: PA3057250410

Gene: F9 HGNC NCBI

ClinVar Allele:

3401358

ClinVar RCV:

RCV004577667

ClinVar Variation:

3242382

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Gly374Ala	CA414446711 NM_001313913.2:c.1121G>C