Canonical Allele Identifier: PA915984343
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val97Asp
CA021206
NM_001258281.1:c.290T>A