Canonical Allele Identifier: PA2827251336
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003171
ClinVar RCV Id: RCV001299693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Gly80Arg
CA378382881
NM_001324337.2:c.238G>A
CA378382882
NM_001324337.2:c.238G>C