Canonical Allele Identifier: PA2828751309
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 1256426
ClinVar RCV Id: RCV001663768 RCV001827570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Arg34Cys
CA6909568
NM_001378246.1:c.100C>T