Canonical Allele Identifier: PA2828751442
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 284771
ClinVar RCV Id: RCV000297423 RCV001086671 RCV003957431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Glu180Val
CA6909734
NM_001378246.1:c.539A>T