Canonical Allele Identifier: PA108853
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1330957
ClinVar RCV Id: RCV001802616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Tyr25Cys
CA414920580
NM_000132.4:c.74A>G