Canonical Allele Identifier: PA2826507036
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2912183
ClinVar RCV Id: RCV003654838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Thr71Met
CA5689561
NM_001269039.3:c.212C>T