Canonical Allele Identifier: PA2827383106
Gene: SGCE HGNC NCBI
ClinVar RCV:
RCV001368574
ClinVar Variation:
1059320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333646.1:p.Pro391Ser
CA368228928
NM_001346717.1:c.1171C>T