Canonical Allele Identifier: PA106699
Gene: SLC25A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005975.1:p.Arg282Cys
CA130979
NM_005984.5:c.844C>T