Canonical Allele Identifier: PA2826507180
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499955
ClinVar RCV Id: RCV003224047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser186Leu
CA378386018
NM_001269039.3:c.557C>T