Canonical Allele Identifier: PA2827251321
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 179760
ClinVar RCV Id: RCV000156558 RCV000471315 RCV000680347 RCV001803094 RCV002399558
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser57Phe
CA185080
NM_001324337.2:c.170C>T