Canonical Allele Identifier: PA107351
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10210
ClinVar RCV Id: RCV000010923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Leu431Phe
CA255100
NM_000132.4:c.1293G>T
CA414915298
NM_000132.4:c.1293G>C