Canonical Allele Identifier: PA109058
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10177
ClinVar RCV Id: RCV000010890 RCV000851946 RCV001701720 RCV003398478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val181Met
CA255066
NM_000132.4:c.541G>A