Canonical Allele Identifier: PA2826464221
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140888
ClinVar RCV Id: RCV000129124 RCV000210186 RCV000688403 RCV003477537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn411His
CA018266
NM_001258281.1:c.1231A>C