Canonical Allele Identifier: PA110553
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_000124.1:p.Val228Leu
CA121130
NM_000133.4:c.682G>C