Canonical Allele Identifier: PA2828751198
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 281085
ClinVar RCV Id: RCV000260683 RCV000723533 RCV002265721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Leu194Ser
CA6909795
NM_001378245.1:c.581T>C