Canonical Allele Identifier: PA2828751060
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 289650
ClinVar RCV Id: RCV000366203 RCV001850454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Leu53Pro
CA10606508
NM_001378245.1:c.158T>C