Canonical Allele Identifier: PA2827383238
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333648.1:p.Pro128Leu
CA4348786
NM_001346719.1:c.383C>T