Canonical Allele Identifier: PA185082
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 179760
ClinVar RCV Id: RCV000156558 RCV000471315 RCV000680347 RCV001803094 RCV002399558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser57Phe
CA185080
NM_007373.4:c.170C>T