Canonical Allele Identifier: PA915977436
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 471336
ClinVar RCV Id: RCV000528429 RCV000852721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Asp20Asn
CA8643685
NM_001135697.3:c.58G>A