Canonical Allele Identifier: PA091233
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 217250
ClinVar RCV Id: RCV000201165 RCV000493338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg34Cys
CA210084
NM_000023.3:c.100C>T