Canonical Allele Identifier: PA916063356
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202088
ClinVar RCV Id: RCV000183902 RCV000705812 RCV002408816 RCV002500550 RCV003233490 RCV003317134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Ile64Thr
CA308788
NM_172244.3:c.191T>C