Canonical Allele Identifier: PA2826947042
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10647
ClinVar RCV Id: RCV000011393 RCV001810851
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Gly319Glu
CA255437
NM_001313913.2:c.956G>A