Canonical Allele Identifier: PA2827383018
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2584843
ClinVar RCV Id: RCV003340743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333646.1:p.Ile294Phe
CA4348696
NM_001346717.1:c.880A>T