Canonical Allele Identifier: PA2827383766
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333649.1:p.Asn314Ser
CA368228891
NM_001346720.2:c.941A>G