Canonical Allele Identifier: PA091255
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 285980
ClinVar RCV Id: RCV000388314 RCV003509524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Val196Ile
CA10605322
NM_000023.3:c.586G>A