Canonical Allele Identifier: PA915958362
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 627270
ClinVar RCV Id: RCV000852066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Met633Arg
CA414910260
NM_000132.4:c.1898T>G