Canonical Allele Identifier: PA107872
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10176
ClinVar RCV Id: RCV000010889 RCV003657257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro165Ser
CA255065
NM_000132.4:c.493C>T