Canonical Allele Identifier: PA109216
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 592086
ClinVar RCV Id: RCV000723273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val682Phe
CA414909250
NM_000132.4:c.2044G>T