Canonical Allele Identifier: PA107852
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10244
ClinVar RCV Id: RCV000010957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Phe677Leu
CA255136
NM_000132.4:c.2029T>C
CA414909309
NM_000132.4:c.2031C>G
CA414909311
NM_000132.4:c.2031C>A