Canonical Allele Identifier: PA2828751383
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 595105
ClinVar RCV Id: RCV000730562 RCV003141728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Ser118Pro
CA6909652
NM_001378246.1:c.352T>C