Allele Registry

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Canonical Allele Identifier: PA2580369031

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_031399.2:p.Gly53Arg	CA378381906 NM_007373.4:c.157G>A CA378381911 NM_007373.4:c.157G>C