Canonical Allele Identifier: PA108614
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10306
ClinVar RCV Id: RCV000011019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Trp2065Arg
CA255199
NM_000132.4:c.6193T>C
CA414903308
NM_000132.4:c.6193T>A