Canonical Allele Identifier: PA2826464173
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val397Met
CA16617578
NM_001258281.1:c.1189G>A