Canonical Allele Identifier: PA2826506931
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749309
ClinVar RCV Id: RCV003540262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Pro16Arg
CA5689548
NM_001269039.3:c.47C>G