Canonical Allele Identifier: PA106054
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10171
ClinVar RCV Id: RCV000010884 RCV001529373 RCV002496321 RCV002247319 RCV002280860 RCV003952352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu132Asp
CA255060
NM_000132.4:c.396A>C
CA414919826
NM_000132.4:c.396A>T