Canonical Allele Identifier: PA2826506913
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3161864
ClinVar RCV Id: RCV004451210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Lys7Asn
CA378380286
NM_001269039.3:c.21A>C
CA378380288
NM_001269039.3:c.21A>T