Canonical Allele Identifier: PA2829907306
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10333
ClinVar RCV Id: RCV000011046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Arg188Cys
CA255225
NM_019863.3:c.562C>T