Canonical Allele Identifier: PA2826946930
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10594
ClinVar RCV Id: RCV000011340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Val190Leu
CA121130
NM_001313913.2:c.568G>C