Canonical Allele Identifier: PA207763
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 212138
ClinVar RCV Id: RCV000193940 RCV000873932 RCV001558681 RCV004541252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006633.1:p.Asp501His
CA207762
NM_006642.5:c.1501G>C