Canonical Allele Identifier: PA916071874
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Arg93Gln
CA255016
NM_019863.3:c.278G>A