Canonical Allele Identifier: PA2580116645
Gene: FNDC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2366028
ClinVar RCV Id: RCV004202397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001343.2:p.Arg210Ser
CA3533961
NM_001001343.4:c.630G>C
CA3533962
NM_001001343.4:c.630G>T