Canonical Allele Identifier: PA2826506928
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181526
ClinVar RCV Id: RCV000159108 RCV000519096 RCV001286466 RCV003917545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu13Ala
CA297169
NM_001269039.3:c.38A>C