Canonical Allele Identifier: PA2826507051
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233637
ClinVar RCV Id: RCV004097717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu89Asp
CA378383261
NM_001269039.3:c.267G>C
CA378383266
NM_001269039.3:c.267G>T