Canonical Allele Identifier: PA915977665
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 554420
ClinVar RCV Id: RCV000670049 RCV003155270 RCV003480755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Glu137Gln
CA400179814
NM_001135697.3:c.409G>C