Allele Registry

Canonical Allele Identifier: PA2579921003

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV003182931

ClinVar Variation:

2453476

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu731Lys	CA346729404 NM_000251.3:c.2191G>A