Canonical Allele Identifier: PA107814
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10196
ClinVar RCV Id: RCV000010909 RCV000852250 RCV003656098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Phe312Ser
CA255083
NM_000132.4:c.935T>C