Canonical Allele Identifier: PA107748
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10309
ClinVar RCV Id: RCV000011022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Phe2120Leu
CA255202
NM_000132.4:c.6360T>G
CA414899736
NM_000132.4:c.6360T>A
CA414899758
NM_000132.4:c.6358T>C