Canonical Allele Identifier: PA2580105275
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428751
ClinVar RCV Id: RCV003120352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Cys547Arg
CA414911874
NM_000132.4:c.1639T>C