Canonical Allele Identifier: PA915977474
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 281859
ClinVar RCV Id: RCV000298182 RCV000544017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Ala53Thr
CA8643703
NM_001135697.3:c.157G>A