Canonical Allele Identifier: PA2826463303
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met195Ile
CA346732485
NM_001258281.1:c.585G>A
CA346732487
NM_001258281.1:c.585G>C
CA346732489
NM_001258281.1:c.585G>T