Canonical Allele Identifier: PA915977657
Gene: SGCA HGNC NCBI
ClinVar RCV:
RCV000010045
ClinVar Variation:
9438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Glu137Gly
CA120429
NM_001135697.3:c.410A>G