Canonical Allele Identifier: PA645294571
Gene: F8 HGNC NCBI
ClinVar RCV:
RCV000298078
ClinVar Variation:
368121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asp845Glu
CA10568309
NM_000132.4:c.2535C>A
CA414901490
NM_000132.4:c.2535C>G