Canonical Allele Identifier: PA109234
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10165
ClinVar RCV Id: RCV000010878
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val99Asp
CA255054
NM_000132.4:c.296T>A