Canonical Allele Identifier: PA2826507107
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181527
ClinVar RCV Id: RCV000466484 RCV000763645 RCV002262761 RCV002336368 RCV001813417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile119Val
CA297175
NM_001269039.3:c.355A>G