Canonical Allele Identifier: PA2825133321
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1004253
ClinVar RCV Id: RCV001300929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Pro88Ser
CA362008072
NM_000337.6:c.262C>T