Canonical Allele Identifier: PA915977523
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 436698
ClinVar RCV Id: RCV000499843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Pro70Arg
CA400177397
NM_001135697.3:c.209C>G