Canonical Allele Identifier: PA108732
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10234
ClinVar RCV Id: RCV000010947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Trp604Cys
CA255127
NM_000132.4:c.1812G>C
CA414910930
NM_000132.4:c.1812G>T