Canonical Allele Identifier: PA2580116642
Gene: FNDC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2315183
ClinVar RCV Id: RCV004161117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001343.2:p.Arg210Lys
CA3533963
NM_001001343.4:c.629G>A