Canonical Allele Identifier: PA2829907303
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10147
ClinVar RCV Id: RCV000010860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Pro184Ser
CA255041
NM_019863.3:c.550C>T