Canonical Allele Identifier: PA2826507163
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372586
ClinVar RCV Id: RCV000412927 RCV002481272 RCV002524636 RCV004022163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Arg172Trp
CA16042705
NM_001269039.3:c.514C>T