Canonical Allele Identifier: PA2573189736
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373165
ClinVar RCV Id: RCV001880679 RCV002334780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val89Ile
CA346730527
NM_001258281.1:c.265G>A