Canonical Allele Identifier: PA345391
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90628
ClinVar RCV Id: RCV000478413 RCV000446874 RCV000524340 RCV001001300 RCV001143792 RCV003492421 RCV003997145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr441Pro
CA018000
NM_000251.3:c.1321A>C