Canonical Allele Identifier: PA2826507271
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2183242
ClinVar RCV Id: RCV002615415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Gln229Lys
CA5689609
NM_001269039.3:c.685C>A