Canonical Allele Identifier: PA091240
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 9438
ClinVar RCV Id: RCV000010045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Glu137Gly
CA120429
NM_000023.3:c.410A>G