Canonical Allele Identifier: PA658665536
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 471337
ClinVar RCV Id: RCV000553098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Val242Phe
CA400181014
NM_000023.3:c.724G>T