Canonical Allele Identifier: PA2826943674
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 12056
ClinVar RCV Id: RCV000012836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Val294Met
CA256478666
NM_001312674.2:c.880G>A