Canonical Allele Identifier: PA2826462854
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798272
ClinVar RCV Id: RCV002442086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg33Ile
CA346729617
NM_001258281.1:c.98G>T