Canonical Allele Identifier: PA109160
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10142
ClinVar RCV Id: RCV000010855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val345Leu
CA255036
NM_000132.4:c.1033G>T
CA337336646
NM_000132.4:c.1033G>C