Canonical Allele Identifier: PA308784
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202086
ClinVar RCV Id: RCV000183900 RCV001852377 RCV003233488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Val39Ala
CA308782
NM_000337.6:c.116T>C