Canonical Allele Identifier: PA237512
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_000328.2:p.Tyr90Asn
CA237510
NM_000337.6:c.268T>A