Canonical Allele Identifier: PA2827251400
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Val188Leu
CA378386042
NM_001324337.2:c.562G>T
CA378386044
NM_001324337.2:c.562G>C