Canonical Allele Identifier: PA108364
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10226
ClinVar RCV Id: RCV000010939 RCV000727106 RCV003934821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser554Gly
CA255116
NM_000132.4:c.1660A>G