Canonical Allele Identifier: PA2826507007
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339314
ClinVar RCV Id: RCV002272501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Gly53Arg
CA378381906
NM_001269039.3:c.157G>A
CA378381911
NM_001269039.3:c.157G>C