Canonical Allele Identifier: PA2741818717
Gene: FNDC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2543399
ClinVar RCV Id: RCV004318614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001343.2:p.Asp96Glu
CA3534039
NM_001001343.4:c.288T>A
CA361975165
NM_001001343.4:c.288T>G