Canonical Allele Identifier: PA2826507183
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748749
ClinVar RCV Id: RCV002345078 RCV003539427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Val188Leu
CA378386042
NM_001269039.3:c.562G>T
CA378386044
NM_001269039.3:c.562G>C