Canonical Allele Identifier: PA2826463498
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 848726
ClinVar RCV Id: RCV001052546
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala243Thr
CA041137
NM_001258281.1:c.727G>A