Canonical Allele Identifier: PA2573169869
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1676735
ClinVar RCV Id: RCV002222132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Ile451Leu
CA7060734
NM_000504.4:c.1351A>C