Canonical Allele Identifier: PA199176
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181528
ClinVar RCV Id: RCV000169685 RCV000586119 RCV000523270 RCV001376015 RCV001030821 RCV002336369 RCV003156077
ClinVar Variation Id: 546129
ClinVar RCV Id: RCV000657957
ClinVar Variation Id: 2850800
ClinVar RCV Id: RCV003655985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Met173Ile
CA199174
NM_007373.4:c.519G>A
CA378385803
NM_007373.4:c.519G>T
CA378385809
NM_007373.4:c.519G>C