Canonical Allele Identifier: PA2573074932
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 461622
ClinVar RCV Id: RCV000559899 RCV000593280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365173.1:p.Leu71Phe
CA6909584
NM_001378244.1:c.211C>T