Canonical Allele Identifier: PA658671321
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Met149Val
CA5689591
NM_007373.4:c.445A>G