Canonical Allele Identifier: PA2826507046
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450870
ClinVar RCV Id: RCV003171525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser86Gly
CA378383080
NM_001269039.3:c.256A>G