Canonical Allele Identifier: PA105878
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10202
ClinVar RCV Id: RCV000010915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Cys348Ser
CA255091
NM_000132.4:c.1043G>C
CA414917198
NM_000132.4:c.1042T>A