Allele Registry

Canonical Allele Identifier: PA658672475

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 455498

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met492Ile	CA346727075 NM_000251.3:c.1476G>A CA346727077 NM_000251.3:c.1476G>C CA346727079 NM_000251.3:c.1476G>T