Canonical Allele Identifier: PA2827250940
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760674
ClinVar RCV Id: RCV002409893 RCV003099751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Lys26Arg
CA5689550
NM_001324336.2:c.77A>G