Canonical Allele Identifier: PA2826507045
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2186845
ClinVar RCV Id: RCV002606947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser86Arg
CA213256954
NM_001269039.3:c.258C>A
CA378383081
NM_001269039.3:c.256A>C
CA378383123
NM_001269039.3:c.258C>G