Canonical Allele Identifier: PA299337
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90873
ClinVar RCV Id: RCV000160600 RCV000524374 RCV000586744 RCV003452885
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu687Pro
CA019927
NM_000251.3:c.2060T>C