Canonical Allele Identifier: PA2826463241
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758545
ClinVar RCV Id: RCV002380341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys180Gln
CA022120
NM_001258281.1:c.538A>C