Canonical Allele Identifier: PA2826507225
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 240838
ClinVar RCV Id: RCV000229898 RCV000314432 RCV000479328 RCV001174950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile204Val
CA5689600
NM_001269039.3:c.610A>G