Canonical Allele Identifier: PA104865
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637834
ClinVar RCV Id: RCV003405132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg2169Cys
CA10567800
NM_000132.4:c.6505C>T