Canonical Allele Identifier: PA2826463293
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 841179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu192Phe
CA040395
NM_001258281.1:c.576G>T
CA346732443
NM_001258281.1:c.576G>C