Canonical Allele Identifier: PA255035
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10141
ClinVar RCV Id: RCV000010854
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Cys329Arg
CA255034
NM_000132.4:c.985T>C