Canonical Allele Identifier: PA2826506982
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141254
ClinVar RCV Id: RCV003056863 RCV003994488 RCV004070243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Lys36Arg
CA5689556
NM_001269039.3:c.107A>G