Canonical Allele Identifier: PA2827251287
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749309
ClinVar RCV Id: RCV003540262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Pro16Arg
CA5689548
NM_001324337.2:c.47C>G