Canonical Allele Identifier: PA2741935629
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2503516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Asp49Asn
CA5689558
NM_007373.4:c.145G>A