Canonical Allele Identifier: PA2827251397
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 996269
ClinVar RCV Id: RCV001290609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser186Ala
CA378386010
NM_001324337.2:c.556T>G