Canonical Allele Identifier: PA108316
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10195
ClinVar RCV Id: RCV000010908 RCV003415685
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser308Leu
CA255082
NM_000132.4:c.923C>T