Canonical Allele Identifier: PA106209
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163210
ClinVar RCV Id: RCV001508074 RCV002272475 RCV002246393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu340Lys
CA10568511
NM_000132.4:c.1018G>A