Canonical Allele Identifier: PA2573061410
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1330455
ClinVar RCV Id: RCV001803547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1740Met
CA414913424
NM_000132.4:c.5219G>T