Canonical Allele Identifier: PA2828751518
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 2063856
ClinVar RCV Id: RCV002943016
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Cys267Ser
CA6909849
NM_001378246.1:c.800G>C
CA387503815
NM_001378246.1:c.799T>A
CA658832944
NM_001378246.1:c.[800G>C;801T>C]
CA2580086817
NM_001378246.1:c.800_801delinsCC