Canonical Allele Identifier: PA2741935639
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2725429
ClinVar RCV Id: RCV003540051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Pro79Arg
CA378382866
NM_007373.4:c.236C>G