Canonical Allele Identifier: PA142645
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 48123
ClinVar RCV Id: RCV000041411 RCV000172106 RCV000670909 RCV001522616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Asp239Glu
CA142644
NM_172244.3:c.717C>G
CA362008837
NM_172244.3:c.717C>A