Canonical Allele Identifier: PA658800688
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 532690
ClinVar RCV Id: RCV000639549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Gln95His
CA362008121
NM_000337.6:c.285G>C
CA362008122
NM_000337.6:c.285G>T