Canonical Allele Identifier: PA2827251350
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696297
ClinVar RCV Id: RCV002266441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Met103Ile
CA378383866
NM_001324337.2:c.309G>C
CA378383876
NM_001324337.2:c.309G>T
CA378383883
NM_001324337.2:c.309G>A