Canonical Allele Identifier: PA2573182337
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1443684
ClinVar RCV Id: RCV001981335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Leu5Val
CA400210586
NM_001135697.3:c.13C>G