Canonical Allele Identifier: PA915977546
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 659203
ClinVar RCV Id: RCV000816168 RCV002235336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Leu89Phe
CA400177739
NM_001135697.3:c.265C>T