Canonical Allele Identifier: PA645294487
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.His1146Gln
CA1233910
NM_000130.5:c.3438C>G
CA343117892
NM_000130.5:c.3438C>A