Canonical Allele Identifier: PA108225
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1330883
ClinVar RCV Id: RCV001802542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser19Arg
CA414920619
NM_000132.4:c.57T>G
CA414920620
NM_000132.4:c.57T>A
CA414920626
NM_000132.4:c.55A>C