Canonical Allele Identifier: PA2826507038
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014118
ClinVar RCV Id: RCV001312811 RCV003135959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ala78Val
CA5689564
NM_001269039.3:c.233C>T