Allele Registry

Canonical Allele Identifier: PA2579911993

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002359701

ClinVar Variation:

1749593

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln193Lys	CA346730972 NM_000251.3:c.577C>A