Canonical Allele Identifier: PA2828751169
Gene: SGCG HGNC NCBI
ClinVar RCV:
RCV000636846
ClinVar Variation:
530807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Arg166Gln
CA6909702
NM_001378245.1:c.497G>A