Canonical Allele Identifier: PA299383
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182588
ClinVar RCV Id: RCV000160625 RCV000473583 RCV000663301 RCV000562874
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr234Ile
CA022053
NM_000251.3:c.701C>T