Canonical Allele Identifier: PA2826464697
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp531Ala
CA019316
NM_001258281.1:c.1592A>C