Canonical Allele Identifier: PA915977443
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 283448
ClinVar RCV Id: RCV000328161 RCV001083421 RCV001128409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Thr27Met
CA8643689
NM_001135697.3:c.80C>T