Canonical Allele Identifier: PA2573074961
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 311480
ClinVar RCV Id: RCV000271055 RCV000365766 RCV001094118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365173.1:p.Val178Ala
CA6909699
NM_001378244.1:c.533T>C