Canonical Allele Identifier: PA2573162360
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685788
ClinVar RCV Id: RCV002249955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Phe1794Tyr
CA10567975
NM_000132.4:c.5381T>A