Canonical Allele Identifier: PA108985
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1330638
ClinVar RCV Id: RCV001802297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Tyr683Cys
CA414909238
NM_000132.4:c.2048A>G