Canonical Allele Identifier: PA2825782067
Gene: SARDH HGNC NCBI

Linked Data

ClinVar Variation Id: 3157834
ClinVar RCV Id: RCV004450155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128179.1:p.Gly260Asp
CA5314673
NM_001134707.2:c.779G>A