Canonical Allele Identifier: PA891844709
Gene: SGCA HGNC NCBI
ClinVar RCV:
RCV000705659
ClinVar Variation:
581745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg98Gly
CA400177902
NM_000023.3:c.292C>G