Canonical Allele Identifier: PA916071862
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10127
ClinVar RCV Id: RCV000010840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Leu50Ser
CA255028
NM_019863.3:c.149T>C