Canonical Allele Identifier: PA2580116637
Gene: FNDC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2353553
ClinVar RCV Id: RCV004194914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001343.2:p.Pro109Ser
CA3534033
NM_001001343.4:c.325C>T