Canonical Allele Identifier: PA2580369041
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_031399.2:p.Glu89Asp
CA378383261
NM_007373.4:c.267G>C
CA378383266
NM_007373.4:c.267G>T