Canonical Allele Identifier: PA2826465512
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216354
ClinVar Variation Id: 1019094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln727His
CA035514
NM_001258281.1:c.2181G>T
CA346730096
NM_001258281.1:c.2181G>C