Canonical Allele Identifier: PA2579912530
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2994842
ClinVar RCV Id: RCV003858465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr225Pro
CA346731795
NM_000251.3:c.673A>C