Canonical Allele Identifier: PA2826463232
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 433879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu178Ser
CA346732192
NM_001258281.1:c.533T>C