Canonical Allele Identifier: PA2825666851
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 191775
ClinVar RCV Id: RCV000172104 RCV000673652 RCV001303841 RCV003233482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Tyr89Asn
CA237510
NM_001128209.2:c.265T>A