Canonical Allele Identifier: PA2826943701
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1676735
ClinVar RCV Id: RCV002222132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Ile407Leu
CA7060734
NM_001312674.2:c.1219A>C