Canonical Allele Identifier: PA2827251345
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233637
ClinVar RCV Id: RCV004097717
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Glu89Asp
CA378383261
NM_001324337.2:c.267G>C
CA378383266
NM_001324337.2:c.267G>T