Canonical Allele Identifier: PA1139670135
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 914871
ClinVar RCV Id: RCV001169246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ile265Val
CA414918474
NM_000132.4:c.793A>G