Canonical Allele Identifier: PA2826464843
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly562Val
CA16617594
NM_001258281.1:c.1685G>T