Canonical Allele Identifier: PA2580116633
Gene: FNDC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2463686
ClinVar RCV Id: RCV004255681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001343.2:p.His87Arg
CA3534048
NM_001001343.4:c.260A>G