Canonical Allele Identifier: PA1139753145
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 959625
ClinVar RCV Id: RCV001233009 RCV003166428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Val141Leu
CA362010420
NM_172244.3:c.421G>C
CA362010422
NM_172244.3:c.421G>T