Canonical Allele Identifier: PA915957846
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 716179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Arg372Pro
CA7060689
NM_000504.4:c.1115G>C