Canonical Allele Identifier: PA2580369038
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450870
ClinVar RCV Id: RCV003171525
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser86Gly
CA378383080
NM_007373.4:c.256A>G