Canonical Allele Identifier: PA2828066454
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Leu105Arg
CA253601
NM_001362808.2:c.314T>G