Canonical Allele Identifier: PA091235
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 188811
ClinVar RCV Id: RCV000169146 RCV003330528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg74Trp
CA199069
NM_000023.3:c.220C>T