Canonical Allele Identifier: PA2826464828
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428539
ClinVar RCV Id: RCV000492007
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile558Ser
CA346728486
NM_001258281.1:c.1673T>G