Canonical Allele Identifier: PA104885
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10318
ClinVar RCV Id: RCV000011031 RCV003103985
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg2178Cys
CA255211
NM_000132.4:c.6532C>T