Canonical Allele Identifier: PA913191698
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 618106
ClinVar RCV Id: RCV000756116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly2107Asp
CA414900052
NM_000132.4:c.6320G>A