Canonical Allele Identifier: PA2826465875
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489942
ClinVar RCV Id: RCV000580301 RCV000629841 RCV001193286 RCV002245022 RCV004001259
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile817Met
CA037199
NM_001258281.1:c.2451T>G