Canonical Allele Identifier: PA239878
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 194077
ClinVar RCV Id: RCV000174354 RCV001085070 RCV004539611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006633.1:p.Gln460His
CA239877
NM_006642.5:c.1380G>C
CA345475846
NM_006642.5:c.1380G>T