Canonical Allele Identifier: PA2826943692
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091380
ClinVar RCV Id: RCV004385766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Lys366Gln
CA388793789
NM_001312674.2:c.1096A>C