Canonical Allele Identifier: PA2828066963
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1063416
ClinVar RCV Id: RCV001373249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349738.1:p.Pro349Ala
CA162920306
NM_001362809.2:c.1045C>G