Canonical Allele Identifier: PA1139744592
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 92655
ClinVar RCV Id: RCV000078405 RCV000270116 RCV000325049 RCV001094097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365173.1:p.Arg134His
CA145903
NM_001378244.1:c.401G>A