Canonical Allele Identifier: PA308781
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202085
ClinVar RCV Id: RCV000183899 RCV000331989 RCV000389000 RCV000639556 RCV001170139 RCV001701634 RCV003233487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Glu5Asp
CA308779
NM_000337.6:c.15G>C
CA362007517
NM_000337.6:c.15G>T