Canonical Allele Identifier: PA2826465610
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 202204
ClinVar RCV Id: RCV000184050 RCV000466235 RCV000561295 RCV000708845
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly754Asp
CA020624
NM_001258281.1:c.2261G>A