Canonical Allele Identifier: PA2826463900
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408522
ClinVar RCV Id: RCV000458164 RCV001143790 RCV003129864 RCV004022694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala332Val
CA16610785
NM_001258281.1:c.995C>T